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Search results “From chains to bonds”
From Chains to Bonds (Cutscene) - Kingdom Hearts III (Gamerip)
 
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Playlist : https://www.youtube.com/playlist?list=PLWCkhGoFcFizfoiglnETDDgE2i5OCC97D The gamerip is not mine. I simply took the existing .wav files from someone, and edited them if necessary (looping the short tracks, adding a fadeout...), and also ordered them all by approximate order ingame. Check the playlist for more. I recommend you to check the official soundtrack out for a better experience once it's out !
Views: 194 Fivda's Upload Mess
Carbon and its Compounds | Diversity in Carbon bonds | Saturated and un-saturated compunds
 
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CBSE class 10 Science - Carbon and its Compounds - Catenation is the unique property of carbon. It is the self linking of carbon atoms through covalent bonds to form long chains. The carbon atoms can form Straight chain, Branched chain and Ring chain. Saturated Hydrocarbon - Carbon compounds liked with single bond Unsaturated hydrocarbon - Carbon compounds linked with double or triple bond. Bond formed by carbon is highly stable. Prefix of carbon compounds is based on number of carbon atoms and Suffix of carbon compounds depend on the type of bond About PrepOngo: Best Online Learning App which provides CBSE class 10 interactive video lectures, NCERT solutions, written study material, solved examples, in chapter quizzes and practice problems for Science (Physics, Chemistry, Biology) and Mathematics. We try to help the students understand lessons by visualising the concepts through illustrative and interactive videos, practice from large question banks and evaluate and improve yourself continuously. Online Live courses are also offered for CBSE boards, JEE Mains, JEE-Advanced, NEET and Board preparation for class 10, 11 and 12 For all CBSE class 10 Science and Maths video lectures download the Android App: https://goo.gl/HJwkhw Subscribe to our YouTube Channel: https://goo.gl/KSsWP2
Views: 27285 PrepOnGo
Fasting to Break the Bonds of Wickedness and Undo the Heavy Burdens!
 
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In this message, we will discuss how fasting breaks the power of sin and bondages off of our lives and sets us free from oppression, depression, and anxiety in our lives! Follow Us: http://endtimeheadlines.org/about/ Make a Donation: http://endtimeheadlines.org/partner-with-eth/
The Search - From Bonds To Chains
 
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From album: The Search (2004) Label: Self Released
Views: 35 rw104
STRUCTURE OF DNA
 
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For more information: http://www.7activestudio.com [email protected] http://www.7activemedical.com/ [email protected] http://www.sciencetuts.com/ [email protected] Contact: +91- 9700061777, 040-64501777 / 65864777 7 Active Technology Solutions Pvt.Ltd. is an educational 3D digital content provider for K-12. We also customise the content as per your requirement for companies platform providers colleges etc . 7 Active driving force "The Joy of Happy Learning" -- is what makes difference from other digital content providers. We consider Student needs, Lecturer needs and College needs in designing the 3D & 2D Animated Video Lectures. We are carrying a huge 3D Digital Library ready to use. Structure of DNA: The DNA molecule is a polymer consisting of several thousand pairs of nucleotide monomers.Each nucleotide consists of three components. They are 1. Pentose sugar deoxyribose 2. Phosphate group 3. Nitrogenous base Nucleoside = deoxyribose + nitrogenous base Nucleotide = deoxyribose + nitrogenous base + phosphate Pentose sugar:deoxyribose sugar is a pentose sugar with five carbon atoms. Phosphate: the phosphate is attached to the adjacent pentose sugar alternately at their 5th and 3rd carbon atoms by phospho -- diester bonds. The phosphate and pentose sugar constitute the back bone of nucleic acids. Nitrogen bases: there are two types of nitrogen bases 1.Purines adenine and guanine and 2.Pyramidines cytosine and thymine Nitrogenous base is linked to the pentose sugar through N- glycosidic linkage to form a nucleoside. When a phosphate is linked to 51 OH of a nucleoside through phosphoester linkage a corresponding nucleotide is formed. Two nucleotides are linked through 31 -- 51 phosphodiester linkage to form dinucleotide. More nucleotides are joined to form a polynucleotide chain. A polymer has at one end a free phosphate moiety at 51 end of ribose sugar, at the other end the ribose sugar has 31 OH group. The back bone in a polynucleotide chain formed due to sugar and phosphates. The nitrogenous bases linked to sugar moiety form the back bone.
Views: 53168 7activestudio
UCSFChimera: Selectiing atoms, residues and chains
 
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Learn how to select parts of a protein structure using UCSF Chimera.
Views: 19063 RCSBProteinDataBank
American Nomads
 
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http://www.GnosticWarrior.com - A cool BBC Documentary called America Nomads. People who roam the South West free from the bonds and chains of normal every day life
Views: 2182255 Gnostic Warrior
Breaking Chains
 
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In this video, Easwaran talks about the inner bonds of rigid likes and dislikes that limit our ability to concentrate, to make positive changes, and to feel comfortable and secure with ourselves and others.
Views: 4658 Eknath Easwaran
Unsaturated vs Saturated vs Trans Fats, Animation
 
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Chemistry and biology of different types of fat. Why trans-fats are so bad? This video and other related images/videos (in HD) are available for instant download licensing here: https://www.alilamedicalmedia.com/-/galleries/images-videos-by-medical-specialties/cardiology-and-vascular-diseases ©Alila Medical Media. All rights reserved. Voice by Ashley Fleming Support us on Patreon and get FREE downloads and other great rewards: patreon.com/AlilaMedicalMedia/posts All images/videos by Alila Medical Media are for information purposes ONLY and are NOT intended to replace professional medical advice, diagnosis or treatment. Always seek the advice of a qualified healthcare provider with any questions you may have regarding a medical condition. Contrary to popular belief, not all fats cause heart diseases and are bad. In fact, most fats, in adequate amounts, are required for normal bodily functions, especially brain functions. There are also good fats that actually decrease the risks for cardiovascular diseases. A fat molecule is composed of a glycerol head and three fatty acid tails, each of which is a long hydrocarbon chain - a carbon skeleton bound to hydrogen atoms. When all the carbons are fully bound to hydrogens, the fatty acid is said to be saturated - all the bonds between carbon atoms are single, and the hydrocarbon chain has a straight shape. A fat molecule made entirely of saturated fatty acids is a saturated fat. Due to their straight tails, saturated fats are compact and solid at room temperature. On the other hand, when the hydrocarbon chain has fewer hydrogens, it is said to be unsaturated. Instead of binding to a maximum number of hydrogens, some carbon atoms bind to each other via a double bond. The presence of double bonds may bend the hydrocarbon chain, creating gaps between molecules, making them less compact. As a result, unsaturated fats are usually liquid at room temperature. A fat molecule that contains only one double bond is a monounsaturated fat, while one that has multiple double bonds is polyunsaturated. Dietary fats provide fatty acids for the synthesis of the cell membrane - a vital component of all animal cells. The gaps in unsaturated fatty acids provide membrane fluidity, facilitating membrane transport and cellular signaling. While both types of fats are needed for an optimal composition of the cell membrane, too much saturated fat, which is commonly the case in a typical American diet, would make the membrane rigid and hinder cellular responsiveness. Membrane fluidity is most important in the nervous system, where neuronal response requires extremely fast cellular communication. A certain ratio of unsaturated to saturated fatty acids is also required for the formation of myelin – the insulating material that wraps around axons of neurons and speeds up the conduction of electrical signals. The body is capable of synthesizing all the fatty acids it needs, with the exception of polyunsaturated fatty acids omega-3 and omega-6, which must be obtained from the diet. These are known as essential fatty acids. In general, unsaturated fats are healthier than saturated fats. Unsaturated fats decrease the risks for heart disease by reducing the amount of bad cholesterol, LDL, and increasing the good cholesterol, HDL; while saturated fats increase both good and bad cholesterol. But not all unsaturated fats are equal. In fact, a type of unsaturated fat, known as trans-fat, is the unhealthiest of all! A double bond can give rise to 2 possible configurations: cis and trans. Cis is when the 2 hydrogen atoms are on the same side of the bond, while trans is when they are on the opposite sides. A cis double bond bends the fatty acid molecule, while the somewhat more symmetric trans configuration does not. A trans-fat is therefore similar in structure to a saturated fat. More importantly, trans-fats rarely occur in nature so the body does not have the necessary enzymes to break them down. Diets rich in trans-fats increase the bad cholesterol LDL and reduce the good cholesterol HDL, having the most detrimental effect on blood vessels. Trans-fats are found mainly in partially hydrogenated oil products, such as margarine. Because unsaturated fats are less stable and spoil faster, food manufacturers add hydrogens to make them more saturated through a process known as partial hydrogenation. This process not only prolongs shelf-life of vegetable oils, but also turns them into solid, or semi-solid products, which are preferred by commercial bakers for their low cost and wide range of different textures. Unfortunately, partial hydrogenation also converts some of the cis double bonds into trans configuration, producing trans-fats.
Views: 13938 Alila Medical Media
The Peptide Bond: Formation and Cleavage
 
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How is the peptide bond formed and how can it be cleaved?
Views: 28558 khanacademymedicine
TetR D H-Bonds Simulation
 
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TetR D (with 7 missing AS on chain A and 8 missing AS on chain B, due to .pdb file) was simulated in std. forcefield to analyze H-bond interactions. This is just a preview bec. no codecs are installed on this machine :) vmd setups: - coloration with beta-factors, blue/green - sidechains of h-bonds coloured by chain A and chain B (red/orange)
Views: 103 Harry Mampf
Peptide bonds: Formation and cleavage | Chemical processes | MCAT | Khan Academy
 
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Peptide bonds are formed when the amine group of one amino acid binds with the carbonyl carbon of another amino acid. We will learn more about peptide bonds and how the cleaving process occurs. By Tracy Kovach. Created by Tracy Kim Kovach. Watch the next lesson: https://www.khanacademy.org/test-prep/mcat/chemical-processes/amino-acids-peptides-proteins-5d/v/special-cases-histidine-proline-glycine-cysteine?utm_source=YT&utm_medium=Desc&utm_campaign=mcat Missed the previous lesson? https://www.khanacademy.org/test-prep/mcat/chemical-processes/amino-acids-peptides-proteins-5d/v/central-dogma-revisited?utm_source=YT&utm_medium=Desc&utm_campaign=mcat MCAT on Khan Academy: Go ahead and practice some passage-based questions! About Khan Academy: Khan Academy offers practice exercises, instructional videos, and a personalized learning dashboard that empower learners to study at their own pace in and outside of the classroom. We tackle math, science, computer programming, history, art history, economics, and more. Our math missions guide learners from kindergarten to calculus using state-of-the-art, adaptive technology that identifies strengths and learning gaps. We've also partnered with institutions like NASA, The Museum of Modern Art, The California Academy of Sciences, and MIT to offer specialized content. For free. For everyone. Forever. #YouCanLearnAnything Subscribe to Khan Academy’s MCAT channel: https://www.youtube.com/channel/UCDkK5wqSuwDlJ3_nl3rgdiQ?sub_confirmation=1 Subscribe to Khan Academy: https://www.youtube.com/subscription_center?add_user=khanacademy
Views: 255285 khanacademymedicine
The Search - From Bonds To Chains (live @ TIC - The Inner Circle, March 2012)
 
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Band: The Search Song: From Bonds To Chains Venue: T.I.C. - The Inner Circle (Mülheim an der Ruhr) Date: 31.03.2012 Special thanks to the club, the guests and everyone out there
Views: 248 Frank van Düren
Making Sense of Chemical Structures
 
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Drawings and naming organic molecules leads to mass confusion for Biology students, most of whom have not yet taken Organic Chemistry. This video will introduce you to this strange world filled with chains and rings and help you to make sense of it. If you have watched my CHEMISTRY BASICS videos I and II (links below) you are ready for what comes next! By the end of the video you will be able to look at structures for aspirin and caffeine and figure out the chemical formula for each. YES YOU WILL!!! Links to CHEMISTRY BASICS VIDEOS Chemistry Basics Part I: http://youtu.be/MYuh5yErdfA Chemistry Basics Part II: http://youtu.be/Juw7HBg0zZs JOIN THE FUN all over the WEB: SUBSCRIBE: http://www.youtube.com/user/ThePenguinProf FACEBOOK: https://www.facebook.com/ThePenguinProf GOOGLE+: https://plus.google.com/+Penguinprof/posts TWITTER: https://twitter.com/penguinprof WEB: http://www.penguinprof.com/ VIDEO DETAILS: Feel the Power of STRUCTURES Recall: Bonding Rules are based on valence electrons Hydrogen: happy with 1 covalent bond Carbon: happy with 4 covalent bonds Nitrogen: happy with 3 covalent bonds Oxygen: happy with 2 covalent bonds Organic chemistry codifies lots of things: How Many Carbons? Types of Carbon-Carbon Bonds Let's get drawing and understanding: Ethanol: (structure to formula: C2H6O Ethanol has two carbon atoms (eth-) with a single bond between them (-ane), and an attached -OH group (suffix "-ol") RULES: 1. Carbon lives at BENDS and ENDS 2. HYDROGENS bring carbon HAPPINESS Let's try another: Caffeine (structure to formula): C8H10N4O2 And finally: Aspirin: (structure to formula): C9H8O4
Views: 196824 ThePenguinProf
Break free of Life's bonds & begin a life of freedom
 
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3 strands of #12 Jack Chain broken with the Ironmind neck harness.....Practice / revision #2 of "Breaking the chains of bondage". If you want to be one of the first to see this live, then Join us @ Chriistian World on Sunday, Oct 30 @ 10AM in Children's World.
Views: 118 Jeff Bankens
Naming carbon chains
 
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Naming chains with alcohols and double bonds :)
Views: 560 hummyp
Immunology - Antibody Structure & Function
 
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Antibodies, also known as immunoglobulins, are like the ammunition of the body’s humoral defense against microorganisms. Plasma cells are like the turret guns of the immune system that secrete thousands of antibodies per second. You should know the general structure of the 5 types of antibodies, as well as the specific structure of an individual antibody. First, I’m going to draw a 2 by 2 grid to demonstrate the difference between the light and heavy chains, as well as the variable and constant regions. Each antibody has 2 light chains with a variable region known as V-L and a constant region known as C-L. Each heavy has a variable region known as V-H and three constant regions known as C-H-1, C-H-2, and C-H-3. Disulfide bonds join the light chain to the heavy chain here, and the heavy chains of IgG to each other here. These disulfide bonds bend here at the Hinge region so that the overall antibody structure forms a Y shape. Four regions, V-L, C-L, V-H, and C-H-1 make up the fragment of antigen binding, or Fab. The variable regions of the Fab fragment determine the specific idiotype: the unique structure of which binds to a corresponding specific antigen. Each B cell expresses only one idiotype of an antibody. As an example, a lab-made immune Fab specific to digoxin is used as an antidote to overdoses of the medication. C-H-2 and C-H-3 together make up the Fc region of the antibody, which corresponds to the stalk of the Y. C-H-2 has the special property of binding to complement, something I will cover in a future video. Now let’s discuss the different isotypes of immunoglobulins. There are 5 types: IgG, IgE, IgD, IgM, and IgA. They are differentiated biochemically by their Fc regions and their different functions. All have monomer forms, but only IgA and IgM have different forms when secreted. IgM can exist as a pentamer linked together by disulfide bonds and a J chain, or joining chain. IgA can exist as a dimer with a J chain as well as a Secretory protein. If you were to know just very simple associations to each type then know these. IgM – Immediate response. IgG – delayed response. IgA – mucous membranes. IgE – allergies and parasites. IgD – unclear function. Question: how many binding sites exist on secreted IgM? Think carefully! Most people’s initial reaction is to say five because secretory IgM exists as a pentamer. However, it is important to remember that each antibody monomer has two binding sites, and thus, secretory IgM has 2 times 5 = 10 binding sites. Thanks for watching! Be sure to like and subscribe for more.
Views: 7523 DrawItKnowIt
How to Draw Skeletal Structure or Bond-Line Notation for Organic Molecules
 
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http://leah4sci.com/skeletal presents: How to Draw Skeletal Structures for Organic Compounds Need help with orgo? Download my free guide '10 Secrets to Acing Organic Chemistry' HERE: http://leah4sci.com/orgo-ebook/ This video shows you how to draw complex organic chemistry molecules in simple skeletal structure or bond-line notation. You'll also learn how to read and understand molecules when written as a bunch of lines and atoms. Want more practice drawing skeletal structures? Try the skeletal practice quiz on my website: http://leah4sci.com/skeletal For more in-depth review including practice problems and explanations, check out my online membership site: http://studyhall.leah4sci.com/join For private online tutoring visit my website: http://leah4sci.com/organic-chemistry-tutor/ Finally, for questions and comments, find me on social media here: Facebook: https://www.facebook.com/Leah4sci Twitter: https://twitter.com/Leah4Sci Google+ https://plus.google.com/u/0/+LeahFisch Pinterest: http://www.pinterest.com/leah4sci/
Views: 124277 Leah4sci
Lipids (Part 2 of 11) - Free Fatty Acids - Intro and Properties
 
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Moof's Medical Biochemistry Video Course: http://moof-university.thinkific.com/courses/medical-biochemistry-for-usmle-step-1-exam Questions Answered in This Video: - What are free fatty acids? - What is(are) the function(s) of fatty acids? - Why can fatty acids be used for fuel? - What is the general structure of a fatty acid? - How are fatty acids classified or categorized? - What is(are) the difference(s) between a saturated and unsaturated fatty acid? - What are cis- and trans- fatty acids? - How do chain length and degree of unsaturation relate to melting points of fats? Don't forget to LIKE, COMMENT, and SUBSCRIBE: http://www.youtube.com/subscription_center?add_user=MoofUniversity INFORMATION ABOUT TUTORING: http://www.moofuniversity.com/tutoring/ TO SUPPORT MOOF UNIVERSITY WITH A FINANCIAL CONTRIBUTION: http://www.moofuniversity.com/support-moof/ INSTAGRAM: https://instagram.com/moofuniversity/ FACEBOOK: https://www.facebook.com/pages/Moof-University/1554858934727545 TWITTER: https://twitter.com/moofuniversity Video Content Summary: Free fatty acids are hydrocarbon chains with a carboxylic acid head group and are amphipathic / amphiphilic because of this. They are highly-reduced molecules (more highly reduced than carbohydrates), rich in electrons, and are thus used as fuel. They also function as an important building block for various membrane lipids. At biological pH levels, the carboxylic acid group exists predominantly in its deprotonated carboxylate form. Most often, fatty acids contain an even number of carbon atoms, usually between 4 and 36. Fatty acids are initially classified by the presence or absence of carbon-carbon double bonds in their hydrocarbon chain. Fatty acids that contain zero carbon-carbon double bonds are known as saturated fatty acids - as they are "saturated" with hydrogens. Fatty acids that contain at least one carbon-carbon double bond are known as unsaturated fatty acids. Unsaturated fatty acids can be further classified based on 1) the geometry of the double bond(s) contained within the hydrocarbon chain and/or 2) the number of carbon-carbon double bonds in the hydrocarbon chain. If the carbon-carbon double bond(s) is (are) cis, we have a cis-unsaturated fatty acid, otherwise known simply as a cis fatty acid. If the carbon-carbon double bond(s) is (are) trans, we have a trans-unsaturated fatty acid, otherwise known simply as a trans fatty acid. Further, fatty acids are monounsaturated fatty acids (MUFAs), if they have only one carbon-carbon double bond in the hydrocarbon chain, and polyunsaturated fatty acids (PUFAs), if they have two or more carbon-carbon double bonds in the hydrocarbon chain. Two factors relating to the structures of fatty acids are important to consider when thinking about the melting point of fats: 1) fatty acid chain length and 2) degree of unsaturation / number of cis carbon-carbon double bonds. An increase in chain length increases the number of atoms that can form temporary dipoles, which increases Van der Waals interactions, and thus, increases melting point. A increase in the degree of unsaturation, specifically, an increase in the number of cis double bonds in a fatty acid, will decrease the ability of atoms to form temporary dipoles and thus, decreases Van der Waals interactions and thus, decreases melting point. This is caused by kinks or bends that form in the hydrocarbon chain of a fatty acid due to a cis carbon-carbon double bond. Kinks or bends to not form with trans fatty acids, and they tend to keep a fairly straight chain, similar in structure to that of a saturated fatty acid.
Views: 24280 Moof University
Hydrogen Bonding and Common Mistakes
 
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To see all my Chemistry videos, check out http://socratic.org/chemistry Hydrogen bonding can be so confusing, and in this video we talk about some common mistakes. Hydrogen bonds are intermolecular forces between molecules. They form because one atom has a high electronegativity, so it gets a partial negative charge, and the hydrogen gets a partial positive charge.
Views: 539632 Tyler DeWitt
The Structure and Properties of Polymers
 
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The Structure and Properties of Polymers Addition polymerisation structure of polymers Monomers contain C=C bonds Double bond opens to (link) bond to next monomer molecule Chain forms when same basic unit is repeated over and over. properties of polymers Modern polymers also developed based on alkynes R-C C - R’ Copolymerisation when more than one monomer is used. Covalent Properties polymer chain length properties An irregular chain structure will result eg propene/ethene/propene/propene/ethene Why might polymers designers want to design a polymer in this way? Polymer (Hint) Intermolecular bonds! Elastomers, plastics & fibres Find a definition and suggest your own example of each of these. What decides the properties of a polymer? Stronger attractive forces between chains = stronger, less flexible polymer. Chains able to slide past each other = flexible polymer . In poly(ethene) attractive forces are weak instantaneous dipole - induced dipole, will it be flexible or not? Properties Of Polymers Nylon has strong hydrogen bonds, why does this make it a strong fibre? Getting ideas straight Look at page 110 -111 of Chemical Ideas. Take turns in explaining to a partner how the following molecular structures affect the overall properties of polymers :- chain length, different side groups, chain branching, stereoregularity, chain flexibility, cross linking. Thermoplastics (80%) No cross links between chains. Weak attractive forces between chains broken by warming. Change shape - can be remoulded. Weak forces reform in new shape when cold. Thermosets Extensive cross-linking formed by covalent bonds. Bonds prevent chains moving relative to each other. What will the properties of this type of plastic be like? Longer chains make stronger polymers. Critical length needed before strength increases. Hydrocarbon polymers average of 100 repeating units necessary but only 40 for nylons. Tensile strength measures the forces needed to snap a polymer. More tangles + more touching!!! Crystalline polymers Areas in polymer where chains packed in regular way. Both amorphous and crystalline areas in same polymer. Crystalline - regular chain structure - no bulky side groups. More crystalline polymer - stronger and less flexible. Cold-drawing When a polymer is stretched a ‘neck’ forms. What happens to the chains in the ‘neck’? Cold drawing is used to increase a polymers’ strength. Why then do the handles of plastic carrier bags snap if you fill them full of tins of beans?
Views: 18434 SliderBase
Polar and NonPolar Molecules: How To Tell If a Molecule is Polar or Nonpolar
 
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This video provides a fast way for you to determine if a molecule is polar or nonpolar. It provides examples so you can quickly distinguish nonpolar molecules from those that are polar. General Chemistry Video Playlist: https://www.youtube.com/watch?v=bka20Q9TN6M&list=PL0o_zxa4K1BV-uX6wXQgyqZXvRd0tUUV0&index=3 Access to Premium Videos: https://www.patreon.com/MathScienceTutor Facebook: https://www.facebook.com/MathScienceTutoring/ Here is a list of molecules that are classified as polar or nonpolar: N2, O2, Cl2, F2, H2 He, Ne, Ar, Xe CH4, C2H6, CH2=CH2, CF4, SBr6, BH3, CO2, PCl5, H2O, NH3, HF, CH3OH, CH3NH2, CH3COOH OCS, CH3F, SO2
Karma Release - Liberation from Karmic Chains - Dissolve Karma
 
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To be able to continue this work and to make it sustainable I need your support. I have created a Patreon page for this here: https://www.patreon.com/elkeneher Other ways to support my work: *** Downloads of the Recordings and more: https://www.freedomconsciousness.com/store/ *** Support my work by buying me a virtual cup of coffee (every little bit helps): https://www.paypal.com/cgi-bin/webscr?cmd=_s-xclick&hosted_button_id=JF6LFJJL9ZNG2 *** Personal Recordings and Assistance: https://www.freedomconsciousness.com/personal-assistance/ Free yourself from Karmic bonds and chains. This recording is designed to release all old karma, that has been running your life. Karma has been very real for eons and now as the paradigm is shifting, Karma is being dissolved as part of the process. This recording will help to speed up the process of dissolving any remaining old Karma that still exists within your life. The law of of cause and effect still applies. So if you want to see good things in your life I recommend to do and be what to want to see. Headphones are not required. Connect with me on Facebook: https://www.facebook.com/elke.neher1 I am using beneficial frequencies and tones combined with a powerful energy transmission that are embedded in this recording. It is my intention that this video will help to dissolve any remaining Karma. Please now add your intention as well, but try to stay as close as possible to the original intention. The more people will do this, the more powerful this video will become. Sit back, relax and enjoy the music, the energy transmission and the beneficial frequencies. Remember to drink plenty of pure water while and after listening. The energies in this recording are very potent, as a precaution, please refrain from listening if you are: Pregnant Suffering from seizures Wearing a pacemaker Operating any machinery or driving Thank you for watching. :) Infinite Love, Elke Medical Disclaimer: Sound, Frequency and Energy healing are energy based healing methods. This recording is not intended to represent that it is used to diagnose, cure, treat, or prevent any medical problem, physical or psychological disorder, nor is it intended as a substitute for seeking professional health care advice. For legal purposes it is understood that this video has been posted for the purpose of entertainment only. I am not a psychologist, physician, or other licensed health care provider. I strongly advise that you seek professional advice as appropriate before making any health decision. All materials are posted in good faith. The accuracy, validity, effectiveness, completeness, or usefulness of any information herein, as with any publication, cannot be guaranteed. Elke Neher accepts no responsibility or liability whatsoever for the use or misuse of the material provided here.
Views: 121106 Elke Neher
Polar & Non-Polar Molecules: Crash Course Chemistry #23
 
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*** PLEASE WATCH WITH ANNOTATIONS ON! SOME INACCURACIES IN GRAPHICS ARE NOTED AND CORRECTED IN ANNOTATIONS. THANKS! *** Molecules come in infinite varieties, so in order to help the complicated chemical world make a little more sense, we classify and categorize them. One of the most important of those classifications is whether a molecule is polar or non-polar, which describes a kind of symmetry - not just of the molecule, but of the charge. In this edition of Crash Course Chemistry, Hank comes out for Team Polar, and describes why these molecules are so interesting to him. You'll learn that molecules need to have both charge asymmetry and geometric asymmetry to be polar, and that charge asymmetry is caused by a difference in electronegativities. You'll also learn how to notate a dipole moment (or charge separation) of a molecule, the physical mechanism behind like dissolves like, and why water is so dang good at fostering life on Earth. -- Table of Contents Charge Assymetry & Geometric Asymmetry 01:33 Difference in Electronegatives 01:49 Hank is Team Polar 00:33 Dipole Moment 03:49 Charge Separation of a Molecule 04:12 Like Dissolves Like 04:41 Water is Awesome 05:10 -- Want to find Crash Course elsewhere on the internet? Facebook - http://www.facebook.com/YouTubeCrashCourse Twitter - http://www.twitter.com/TheCrashCourse Tumblr - http://thecrashcourse.tumblr.com Support CrashCourse on Subbable: http://subbable.com/crashcourse
Views: 2349989 CrashCourse
Carbon and its Compounds | Bonds with other elements | Functional Group
 
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CBSE class 10 Science - Carbon and its Compounds - what is Hetro atom? What are functional group? Hetro atom are which replace the Hydrogen atom from carbon compound. It gives specific chemical property to the compound regardless of the length and nature of the carbon chain. Functional Group - The group of atoms, that are responsible for the chemical properties of a carbon compound. 1. Halogen group 2. Alcoholic group 3. Carboxylic group 4. Aldehyde group 5. Ketone group About PrepOngo: Best Online Learning App which provides CBSE class 10 interactive video lectures, NCERT solutions, written study material, solved examples, in chapter quizzes and practice problems for Science (Physics, Chemistry, Biology) and Mathematics. We try to help the students understand lessons by visualising the concepts through illustrative and interactive videos, practice from large question banks and evaluate and improve yourself continuously. Online Live courses are also offered for CBSE boards, JEE Mains, JEE-Advanced, NEET and Board preparation for class 10, 11 and 12 For all CBSE class 10 Science and Maths video lectures download the Android App: https://goo.gl/HJwkhw Subscribe to our YouTube Channel: https://goo.gl/KSsWP2
Views: 15152 PrepOnGo
From Bonds to Chains
 
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Provided to YouTube by Believe SAS From Bonds to Chains · The Search The Search ℗ Afmusic Released on: 2009-06-01 Author: Razmig Tekeyan Music Publisher: Copyright Control Auto-generated by YouTube.
Views: 24 The Search - Topic
Shackles- The Struggles of a Young Christian (Building Bonds & Breaking Chains Trailer)
 
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Short video depicting the many views of Christianity through the eyes of the youth in the general public. This video also shows real life stuggles of a group of young believers as they try to walk righteous in the eyes of God, and their reasons for pushing through in the faith. This video includes music instrumentals from Exodous 23:1_by: Pusha T Super Human_ by: Andy Mineo Bravo_by Tedashi (Feat) J. Paul
Views: 108 Tyreik Kendell
Hydrocarbons | #aumsum #kids #education #science #learn
 
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Hydrocarbons. Characteristic: Compounds made up of hydrogen and carbon. Hydrocarbons are of 2 types, saturated and unsaturated hydrocarbons. Name: Saturated hydrocarbons. Characteristic: Hydrocarbons in which the carbon atoms are connected by single bonds only. Saturated hydrocarbons are also called Alkanes. Name: Unsaturated hydrocarbons. Characteristic: Hydrocarbons in which the carbon atoms are connected by double bonds or triple bonds are called unsaturated hydrocarbons. Unsaturated hydrocarbons are of 2 types, Alkenes and Alkynes. Name: Alkenes. Characteristic: Unsaturated hydrocarbons in which the carbon atoms are connected by at least one double bond. Name: Alkynes. Characteristic: Unsaturated hydrocarbons in which the carbon atoms are connected by at least one triple bond are called alkynes.
Views: 407188 It's AumSum Time
HOW DID HE GET AWAY?
 
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This video was sponsored by Manscaped.com Get 20% OFF Manscaped + Free Shipping with code MAYO20 at → http://bit.ly/2Mx3V7L GRAB SOME MERCH TO SUPPORT THE SHOW!! http://bit.ly/2rLcMto BECOME A CHANNEL SPONSOR FOR EXCLUSIVE PERKS!- http://bit.ly/2wkm2ah PLEASE SUBSCRIBE! http://bit.ly/1SAml34 Instagram - http://instagram.com/realpatrickthomas Twitter - http://twitter.com/pattymayotv GEAR - BODY ARMOR - SAFELIFEDEFENSE.COM - EVO-RAGE GIMBAL - BY EVOGIMBALS.COM THIS VIDEO IS NOT INTENDED FOR TRAINING, EDUCATION OR ANY OTHER PURPOSE. DO NOT ATTEMPT ANY OF THE ACTIVITIES YOU SEE ON THIS SHOW. THIS SHOW IS NOT AFFILIATED WITH ANY LAW ENFORCEMENT AGENCY.
Views: 2132929 Patty Mayo
SATURATED AND UNSATURATED CARBON COMPOUNDS
 
01:38
For more information: http://www.7activestudio.com [email protected] http://www.7activemedical.com/ [email protected] http://www.sciencetuts.com/ [email protected] Contact: +91- 9700061777, 040-64501777 / 65864777 7 Active Technology Solutions Pvt.Ltd. is an educational 3D digital content provider for K-12. We also customise the content as per your requirement for companies platform providers colleges etc . 7 Active driving force "The Joy of Happy Learning" -- is what makes difference from other digital content providers. We consider Student needs, Lecturer needs and College needs in designing the 3D & 2D Animated Video Lectures. We are carrying a huge 3D Digital Library ready to use. In organic chemistry, a saturated compound is a chemical compound that has a chain of carbon atoms linked together by single bonds. Alkanes as. An unsaturated compound is a chemical compound that contains carbon-carbon double bonds or triple bonds, such as those found in alkenes or alkynes, respectively. Saturated and unsaturated compounds need not consist only of a carbon atom chain. They can form straight chain, branched chain, or ring arrangements. They can have functional groups, as well. It is in this sense that fatty acids are classified as saturated or unsaturated. The amount of unsaturation of a fatty acid can be determined by finding its iodine number.
Views: 21980 7activestudio
Protein Folding Mechanism
 
07:48
Protein folding is the physical process by which a protein chain acquires its native 3-dimensional structure, a conformation that is usually biologically functional, in an expeditious and reproducible manner. It is the physical process by which a polypeptide folds into its characteristic and functional three-dimensional structure from random coil. Each protein exists as an unfolded polypeptide or random coil when translated from a sequence of mRNA to a linear chain of amino acids. This polypeptide lacks any stable (long-lasting) three-dimensional structure (the left hand side of the first figure). As the polypeptide chain is being synthesized by the ribosome, the linear chain begins to fold into its three dimensional structure. Folding begins to occur even during translation of the polypeptide chain. Amino acids interact with each other to produce a well-defined three-dimensional structure, the folded protein (the right hand side of the figure), known as the native state. The resulting three-dimensional structure is determined by the amino acid sequence or primary structure (Anfinsen's dogma).[2] The energy landscape describes the folding pathways in which the unfolded protein is able to assume its native state. Experiments beginning in the 1980s indicate the codon for an amino acid can also influence protein structure. The correct three-dimensional structure is essential to function, although some parts of functional proteins may remain unfolded, so that protein dynamics is important. Failure to fold into native structure generally produces inactive proteins, but in some instances misfolded proteins have modified or toxic functionality. Several neurodegenerative and other diseases are believed to result from the accumulation of amyloid fibrils formed by misfolded proteins. Many allergies are caused by incorrect folding of some proteins, because the immune system does not produce antibodies for certain protein structures. Primary Structure : The primary structure of a protein, its linear amino-acid sequence, determines its native conformation.[7] The specific amino acid residues and their position in the polypeptide chain are the determining factors for which portions of the protein fold closely together and form its three dimensional conformation. The amino acid composition is not as important as the sequence.[8] The essential fact of folding, however, remains that the amino acid sequence of each protein contains the information that specifies both the native structure and the pathway to attain that state. This is not to say that nearly identical amino acid sequences always fold similarly.[9] Conformations differ based on environmental factors as well; similar proteins fold differently based on where they are found. Secondary Structure: Formation of a secondary structure is the first step in the folding process that a protein takes to assume its native structure. Characteristic of secondary structure are the structures known as alpha helices and beta sheets that fold rapidly because they are stabilized by intramolecular hydrogen bonds, as was first characterized by Linus Pauling. Formation of intramolecular hydrogen bonds provides another important contribution to protein stability. Alpha helices are formed by hydrogen bonding of the backbone to form a spiral shape (refer to figure on the right).The beta pleated sheet is a structure that forms with the backbone bending over itself to form the hydrogen bonds (as displayed in the figure to the left). The hydrogen bonds are between the amide hydrogen and carbonyl carbon of the peptide bonds. Tertiary Structure The alpha helices and beta pleated sheets can be amphipathic in nature, or contain a hydrophilic portion and a hydrophobic portion. This property of secondary structures aids in the tertiary structure of a protein in which the folding occurs so that the hydrophilic sides are facing the aqueous environment surrounding the protein and the hydrophobic sides are facing the hydrophobic core of the protein.[11] Secondary structure hierarchically gives way to tertiary structure formation. Once the protein's tertiary structure is formed and stabilized by the hydrophobic interactions, there may also be covalent bonding in the form of disulfide bridges formed between two cysteine residues. Tertiary structure of a protein involves a single polypeptide chain; however, additional interactions of folded polypeptide chains give rise to quaternary structure formation. Chaperone Concept : The Chaperones assist in the correct folding pattern of a protein.If Chaperone fails to do so then Protein ultimately becomes Prion protein which gives rise to several diseases lile Kuru , Scrapie disease and Alziemers.
Views: 35143 Hussain Biology
[Song] Xenogears: chains of ocean and flame (Bonds of fire and Sea) (Chronamut cover)
 
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Xenogears: chains of ocean and flame if you like this, then please subscribe! http://www.youtube.com/user/chronamut?sub_confirmation=1 http://ShawnDall.com (Bonds of fire and Sea) (Chronamut videogame music cover) CLICK THE HQ BUTTON UNDER THE VIDEO! From my 2009 collection: This is a remix of Yasunori Mitsuda's original composition "Chains of Ocean and Flame" - also known as "Bonds of Fire and Sea". you can hear this also at https://soundcloud.com/chronamut/chronamut-xenogears-bonds-of-ocean-sea-vgmix feel free to go there - sign up, and leave me a review! album cover can be viewed at http://chronamut.newgrounds.com/art - along with all my other artwork :) ----- Listen & Buy Chronamut's Music: soundcloud: https://soundcloud.com/chronamut bandcamp: https://chronamut.bandcamp.com/ Spotify: https://play.spotify.com/artist/0qhJLxwvQibBLOAnLLAdPt Itunes: https://itunes.apple.com/ca/album/id1016637148 Amazonmp3: https://www.amazon.com/gp/product/B0113MGLBU?ie=UTF8&camp=1642&creative=6746&creativeASIN=B0113MGLBU&linkCode=as2&tag=musique006-21 Google Play: https://play.google.com/store/music/artist/Chronamut?id=A4kad5glxayjmvylmdqpurmtwsy & many more online store locations! ----- Follow @ Chronamut: music facebook: https://www.facebook.com/KingChronamut art facedbook: https://www.facebook.com/ShawnDallCanadaArtwork spirit facebook: https://www.facebook.com/TheAlmightySource writing facebook: https://www.facebook.com/IAMGODSource twitter: https://twitter.com/Chronamut youtube: http://www.youtube.com/user/chronamut?sub_confirmation=1 updates: https://www.facebook.com/groups/fansofchronamut/ reddit: https://www.reddit.com/r/Chronamut/ forums: http://spiritscienceactivenation.net/Oz/phpBB3/viewforum.php?f=51 charity: gofundme.com/starcrossedlover site: http://ShawnDall.com
Views: 826 Chronamut
Protein Structure (Part 2 of 4) - Secondary Structure - Alpha Helix
 
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Moof's Medical Biochemistry Video Course: http://moof-university.thinkific.com/courses/medical-biochemistry-for-usmle-step-1-exam For Related Practice Problems with Worked Video Solutions on Protein Structure and Function, visit courses.moofuniversity.com. In this video, I explain the details of the alpha helix (alpha helices). The alpha helix is an important type of secondary protein structure. The alpha helix is, specifically, a right handed helix held together by hydrogen bonds (H-bonds) between the carbonyl oxygen and amide hydrogen of the polypeptide backbone. These hydrogen bonds are parallel to the axis of the helix, and they exist between every 4th amino acid of the backbone. The side chains of the amino acids (R-groups) extend out of the helix, running perpendicular to the axis of the helix. The alpha helix is often thought of as having polarity, with the N-terminus (amino terminus) having a partial positive charge, while the C-terminus (carboxy terminus) carries a partial negative charge. There are a few things that can disrupt or damage and alpha helix: 1. Proline – Proline’s side chain is wrapped around and connected to its alpha amino group. This restricts rotation that is necessary to form the particular structure of the alpha helix. Also, when proline’s amino group is part of a peptide bond, it has no hydrogen on it that can hydrogen bond. In short, substituting a proline in for an amino acid that is part of an alpha helix will ruin the alpha helix’s structure. 2. Electrostatic Repulsions between Side Chains with Like Charges – If the R groups of the amino acids that extend outward from the alpha helix happen to be next to each other with like charges, they can repel each other and bend the helix in a way that compromises its structure. For instance, if two negatively charged aspartate side chains are next to each other, they will repel. Likewise, this could occur with two positively charged arginine side chains. 3. Steric Hindrance – The alpha helix is a fairly tightly packed helix, and amino acids with bulky side chains can disrupt its structure by taking up too much space being next to each in the peptide chain that makes up the helix. For example, two phenylalanine side chains next to each other means two aromatic rings (bulky) next to each other. This could disrupt the alpha helix. For a suggested viewing order of the videos, information on tutoring, personalized video solutions, and an opportunity to support Moof University financially, visit MoofUniversity.com, and follow Moof University on the different social media platforms. Don't forget to LIKE, COMMENT, and SUBSCRIBE: http://www.youtube.com/subscription_center?add_user=MoofUniversity SUPPORT MOOF UNIVERSITY: http://www.moofuniversity.com/support-moof/ BUY A T-SHIRT https://shop.spreadshirt.com/moofuniversity/ INFORMATION ABOUT TUTORING AND PERSONALIZED VIDEO SOLUTIONS: http://www.moofuniversity.com/tutoring/ INSTAGRAM: https://instagram.com/moofuniversity/ FACEBOOK: https://www.facebook.com/pages/Moof-University/1554858934727545 TWITTER: https://twitter.com/moofuniversity
Views: 79549 Moof University
Polar and Nonpolar Molecules: Is it Polar or Nonpolar?
 
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This video discusses how to tell if a molecule / compound is polar or nonpolar. Here is a list of molecules that are considered. Subscribe: https://www.youtube.com/channel/UCEWpbFLzoYGPfuWUMFPSaoA?sub_confirmation=1 General Chemistry Video Playlist: https://www.youtube.com/watch?v=bka20Q9TN6M&list=PL0o_zxa4K1BV-uX6wXQgyqZXvRd0tUUV0&index=3 Support: https://www.patreon.com/MathScienceTutor Facebook: https://www.facebook.com/MathScienceTutoring/ Nonpolar Molecules: Diatomic Molecules: H2, N2, O2, Cl2, Br2, F2, I2 Hydrocarbons: CH4, C2H6, C3H8, C2H2, C2H4 Identical Outer Elements With No Lone Pair on Central Atom: Tetrahedral Molecular Geometry: SiBr4, CCl4, CF4, GeH4, CBr4, SiH4 Trigonal Bipyramidal Molecular Geometry: PCl5, PF5, AsF5, PBr5, SbCl5 Linear Molecular Geometry: CO2, CS2, BeH2, BeCl2, and BeF2 Trigonal Planar Molecular Geometry: BH3, AlCl3, AlBr3, AlF3, FeBr3 Octahedral Molecular Geometry: SeF6, SBr6, SF6, SeCl6, SI6, SeI6 Polar Molecules: Same Outer Element With an Assymetrical Lone Pair(s) Bent Molecular Geometry: H2S, H2O, H2Se, SF2, SCl2, SeBr2, SO2, SeO2 Trigonal Pyramidal Molecular Geometry: NH3, PH3, PBr3, PCl3, NF3 T-shaped Molecular Geometry: IF3, ClF3, BrF3, ICl3, BrCl3 Square Pyramidal Molecular Geometry: IF5, ClF5, BrF5, ICl5, BrCl5 SeeSaw Molecular Geometry: SF4, SeCl4, SBr4, SeI4 Exception: XeF4 Different Outer Elements: (Usually Polar) CH3F, CSO, BH2F
Nomenclature - Crash Course Chemistry #44
 
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You can directly support Crash Course at http://www.subbable.com/crashcourse Subscribe for as little as $0 to keep up with everything we're doing. Also, if you can afford to pay a little every month, it really helps us to continue producing great content. Ever feel like there's a international team of bad guys changing all of the easily remembered chemical names and turning them into test-failing, number-infused, pain in the neck names? Well... you're not wrong. IUPAC exists but try to keep in mind that they're doing it for the greater good. In this episode, Hank talks about IUPAC, prefixes, suffixes, ranking, numbers for carbon chains, and cis or trans double bonds. Common Functional Groups: http://en.wikipedia.org/wiki/Functional_group#Table_of_common_functional_groups -- Table of Contents IUPAC 0:00 Every Organic Compound Has Only One Name 1:02 Prefixes 2:16 Suffixes 2:47 Ranking Functional Groups 4:18 Lowest Possible Numbers for Carbon Chains 1:54 Cis or Trans for Double Bonds 6:35 -- Want to find Crash Course elsewhere on the internet? Facebook - http://www.facebook.com/YouTubeCrashCourse Twitter - http://www.twitter.com/TheCrashCourse Tumblr - http://thecrashcourse.tumblr.com Support CrashCourse on Subbable: http://subbable.com/crashcourse
Views: 1021270 CrashCourse
Premium Bonds - time to explain
 
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This is the truth about Premium Bonds... They suck! Whilst this is very UK-centric...there is something like this in every country where your government tell you one thing and use your money in a way that would likely appal you! So Premium Bonds...there are so many reasons why nobody should ever hold a Premium Bond yet somehow 21 million people in the UK are Premium Bond holders! Agree or disagree? Come and join the debate: Facebook - https://www.facebook.com/ThePeoplesGoldMine/ Insta - @peoplesgoldmine Email - [email protected] "It is difficult to free people from the chains they revere" - Voltaire
(shadow bonds) EP 2  schleich wolf movie new 2018
 
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schleich wolf moive. EP 1 https://www.youtube.com/watch?v=kUej06-Vryg&t=86s playlist link https://www.youtube.com/watch?v=7gqDFrDzmt4&list=PLi5SXOIlQgT5VR9mRYr7wdar1F77PWqUf note I am trying to make an original series with a new and unexpected twist.
Views: 2019 Wild Fields
How to Calculate Peptide Charge and Isoelectric Point MCAT Trick
 
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http://leah4sci.com/aminoacids presents: How to calculate peptide charge and Isoelectric Point (pI) without a calculator for the MCAT Is your MCAT just around the corner? Grab a free copy of my ebook "MCAT Exam Strategy - A 6 Week Guide To Crushing The MCAT" at http://mcatexamstrategy.com/ebook This is video 7 in the MCAT amino acids tutorial video series. Learn how to quickly find the charge and isoelectric point of any given dipeptide, tripeptide or even polypeptide without wasting time on useless trial and error calculations. Referenced in this video: Amino Acid pKa table in this tutorial: http://leah4sci.com/amino-acid-charge-in-zwitterions-and-isoelectric-point-mcat-tutorial/ MCAT Math series: http://leah4sci.com/mcatmath Catch this entire video series along with my amino acid cheat sheet, tutorials and practice quiz on my website: http://leah4sci.com/aminoacids Need more help? I offer private online MCAT tutoring. Details http://leah4sci.com/mcat-tutoring/ Have questions? Leave a comment below this video or hit me up on social media: Twitter: http://twitter.com/leah4sci Facebook: https://www.facebook.com/mcatexamstrategy Google+: https://plus.google.com/+LeahFisch/
Views: 106401 Leah4sciMCAT
Organic Chemistry Nomenclature IUPAC Practice Review - Naming Alkanes, Alcohols, Alkenes & Alkynes
 
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This organic chemistry video tutorial provides a review on IUPAC nomenclature. It shows you how to name compounds with functional groups such as alkanes, alcohols, alkenes, alkynes, ethers, carboxylic acids, aldehydes, and ketones. It contains plenty of examples and practice problems that help you if studying for a quiz or if you just to need a complete a homework assignment / worksheet. Here is a list of topics: 1. Alkanes - Methane, Ethane, Propane, Butane, etc. 2. Naming Alkanes With Line Structures 3. Alkyl Substituents - Methyl, Ethyl, Propyl, etc. 4. Nomenclature Rules - priority, alphabetical and numerical order 5. Multiple Alkyl Substituents - Di, Tri, and Tetra Prefixes 6. Complex Substituents 7. Nomenclature of Alkenes - Cis and Trans 8. Nomenclature of Alkynes, Alcohols, and Alkyl Halides 9. How To Find Longest Chain / Parent Chain 10. Naming Cycloalkanes - Cyclopentane & Cyclohexane 11. Cyclohexane Chair Conformation Nomenclature - Cis / Trans Isomers 12. IUPAC Nomenclature of Ethers, Ketones, Aldehydes, and Carboxylic Acids 13. Bridged Bicylic Compounds Nomenclature - How to name it using bridge head carbon atoms 14. R and S Configuration / Stereochemistry Nomenclature 15. Naming Fischer Projections
Carbon and its Compounds (2/4)
 
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Carbon and Compounds (2/4), tetravalency, catenation, isomerism, functional group, IUPAC nomenclature. Subscribe for more
Views: 439195 freakyvikky
Amino Acids and Levels of Protein Structure
 
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Amino Acids and Levels of Protein Structure 1. Introduction 2. Monomers and polymers (dehydration synthesis and hydrolysis reactions) 3. Parts of an amino acid 4. Peptide bonds 5. The way to study amino acids: groups based on shared chemical characteristics 6. Levels of protein structure: Primary: sequence of amino acids Secondary: regions of regular folding due to H-bonds between amino and carboxyl groups that are close together in the polypeptide chain. Alpha helices and beta sheets. And penguins in my kitchen. Tertiary: chemical interactions between R groups Quaternary: interactions between 2 or more polypeptide chains Videos Mentioned: Chemistry Basics I: http://youtu.be/MYuh5yErdfA Chemistry Basics II: http://youtu.be/Juw7HBg0zZs Signal Transduction: http://youtu.be/pH_ibPHK0y0 How Hormones Work: http://youtu.be/KnIu7DDflw8 Just want more Penguin Prof? Subscribe: http://www.youtube.com/user/ThePengui... FB Page: https://www.facebook.com/ThePenguinProf Twitter: https://twitter.com/penguinprof Web: http://www.penguinprof.com/ Penguin Prof is Supported BY AUDIBLE.COM PenguinProf LOVES Audible and now the feeling is mutual! Audible.com is the premier provider of digital audiobooks. Audible has over 150,000 titles to choose from in every genre. Audible titles play on iPhone, Kindle, Android and more than 500 devices for listening anytime, anywhere. Click to learn more and download a FREE audiobook of your choice! http://www.audibletrial.com/PenguinProf
Views: 2192 ThePenguinProf
BRACE FACE EXPOSURE AND BOND CHAIN!
 
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if you have any question about my teeth or anything leave them below!
Views: 1001 Lydia Martinez
Amino Acids
 
05:04
It's time to start learning about all the monomers that make up large biomolecules, and the first one we will look at is the amino acid. These make up proteins, which is most of what you are, so this is pretty important stuff! Subscribe: http://bit.ly/ProfDaveSubscribe [email protected] http://patreon.com/ProfessorDaveExplains http://professordaveexplains.com http://facebook.com/ProfessorDaveExpl... http://twitter.com/DaveExplains General Chemistry Tutorials: http://bit.ly/ProfDaveGenChem Organic Chemistry Tutorials: http://bit.ly/ProfDaveOrgChem Biochemistry Tutorials: http://bit.ly/ProfDaveBiochem Classical Physics Tutorials: http://bit.ly/ProfDavePhysics1 Modern Physics Tutorials: http://bit.ly/ProfDavePhysics2 Mathematics Tutorials: http://bit.ly/ProfDaveMaths Biology Tutorials: http://bit.ly/ProfDaveBio American History Tutorials: http://bit.ly/ProfDaveAmericanHistory
Views: 201364 Professor Dave Explains
Breaking the Chains Bail Bonds FOX Richmond TV Commercial
 
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Call Breaking the Chains Bail Bonds at (804) 536-8848. Serving all Richmond, VA jails anytime. Open 24/7. Call now!
What Are Covalent Bonds | Chemistry for All | FuseSchool
 
05:53
Learn the basics about covalent bonds, when learning about properties of matter. When similar atoms react, like non-metals combining with other non-metals, they share electrons. This is covalent bonding. Non-metals have shells of electrons that are normally half or more than half full of electrons. Since they have a strong attraction for a few additional electrons, it is energetically unfavourable for any of them to lose electrons, so they share electrons by overlapping orbitals. This makes a bonding orbital, or covalent bond, that contains two or more electrons. Covalent bonds can be represented by a dot and cross diagram. These diagrams show only the valence electrons. Covalent bonds are directional, which means they are in a fixed position. The overlap between orbitals mean that the atoms in covalent bonds are very close, and make covalent bonds strong. There are two kinds of covalent structure - small molecules, like water, and giant compounds, like diamond. The electrons in the bonds are evenly shared, which means the bonds are not polarised; there is little attraction between molecules, and forces between molecules are weak. Compounds made from small covalent molecules have low melting and boiling points and are volatile. They also don’t conduct electricity. Carbon and silicon tend to form giant covalent compounds. These bond in the same way, but instead of forming small molecules with one or two bonds, they form four, make up huge lattices or chains of many many linked up atoms. Diamond is a common example, and is made up of Carbon. These compounds have very high melting and boiling points because you have to break covalent bonds rather than intermolecular forces to make them free enough to act like liquids or gases. The covalent bonds hold them rigidly in place in the giant lattice. SUBSCRIBE to the Fuse School YouTube channel for many more educational videos. Our teachers and animators come together to make fun & easy-to-understand videos in Chemistry, Biology, Physics, Maths & ICT. JOIN our platform at www.fuseschool.org This video is part of 'Chemistry for All' - a Chemistry Education project by our Charity Fuse Foundation - the organisation behind The Fuse School. These videos can be used in a flipped classroom model or as a revision aid. Find our other Chemistry videos here: https://www.youtube.com/playlist?list=PLW0gavSzhMlReKGMVfUt6YuNQsO0bqSMV Twitter: https://twitter.com/fuseSchool Access a deeper Learning Experience in the Fuse School platform and app: www.fuseschool.org Follow us: http://www.youtube.com/fuseschool Friend us: http://www.facebook.com/fuseschool This Open Educational Resource is free of charge, under a Creative Commons License: Attribution-NonCommercial CC BY-NC ( View License Deed: http://creativecommons.org/licenses/by-nc/4.0/ ). You are allowed to download the video for nonprofit, educational use. If you would like to modify the video, please contact us: [email protected]
Michael Bolton - Steel Bars
 
03:27
Michael Bolton's official music video for 'Steel Bars'. Click to listen to Michael Bolton on Spotify: http://smarturl.it/MichaelBoltonSpotify?IQid=MichaelBSB As featured on The Essential Michael Bolton. Click to buy the track or album via iTunes: http://smarturl.it/EssentialMichaelB?IQid=MichaelBSB Google Play: http://smarturl.it/MBSBGPlay?IQid=MichaelBSB Amazon: http://smarturl.it/EssentialMBAmazon?IQid=MichaelBSB More From Michael Bolton Missing You Now: https://youtu.be/xo-jCrIRb9g How Am I Supposed To Live Without You: https://youtu.be/YFood_bTOX4 How Can We Be Lovers: https://youtu.be/L0frA_0MjW8 More great 80s videos here: http://smarturl.it/Ultimate80?IQid=MichaelBSB Follow Michael Bolton Facebook: https://www.facebook.com/MBsings Twitter: https://twitter.com/mbsings Subscribe to Michael Bolton on YouTube: http://smarturl.it/MichaelBoltonSub?IQid=MichaelBSB --------- Lyrics: In the night I hear you speak Turn around, you're in my sleep Feel your hands inside my soul You're holding on and you won't let go I've tried running but there's no escape Can't bend them, and I just can't break these.... Steel bars, wrapped all around me I've been your prisoner since the day you found me I'm bound forever, till the end of time Steel bars wrapped around this heart of mine
Views: 5769643 MichaelBoltonVEVO
Amino Acids - What are Amino Acids - What Do Amino Acids Do
 
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In this video I discuss what are amino acids, what are amino acids made of, and what do amino acids do in the body. I also cover what are peptide bonds, polypeptide chains, how amino acids form proteins, some functions of amino acids, and what are amino acids used to build. Transcript We are going to start by looking at the molecular structure of a typical amino acid, don’t worry, I am going to make it easy to understand. The basic structure of amino acids is that they consist of a carboxyl group, a lone hydrogen atom, an amino group, and a side chain, which is often referred to as an R-group. The formation of the side chain is what makes amino acids different from one another. As you can see in this diagram, these 4 are all connected to a carbon atom, which is referred to as the alpha carbon. Not every amino acid follows this exact structure, but, most do. On the screen I have 3 different amino acids, lysine, tryptophan, and leucine. You can see that each has a carboxyl group, an alpha carbon, a amino group, and an R-group that is different from each other. There are 23 total amino acids that are proteinogenic. Proteinogenic amino acids are precursors to proteins, which means they are compounds that participate in a chemical reaction to produce another compound. Of these 23 amino acids, 20 of them are called standard amino acids, and the other 3 are non-standard amino acids. These are listed on the screen. In this video we are going to focus on the standard amino acids, as they are what make up proteins. These amino acids can be classified many different ways, we are going to classify them in a basic nutritional way. Essential and nonessential. Essential amino acids cannot be made by the body, so, they must come from foods we eat. Nonessential amino acids are amino acids that our bodies can produce even if we don’t get them from the food we eat. There is a subgroup of nonessential amino acids that are considered to be conditional amino acids. The list of conditional amino acids is not definitive. For instance, in times of illness or stress, there are certain amino acids the body cant produce sufficiently, and children's bodys haven’t developed the ability to produce certain amino acids yet. There are 9 essential and 11 nonessential amino acids, ive listed them on the screen. So, how do amino acids form proteins? Proteins are built from the 20 standard amino acids. Well, the first thing that happens is that 2 amino acids come together to form a peptide bond. A peptide bond is when the carboxyl group of one amino acid bonds with the amino group of another amino acid, as you can see here. If you notice 2 hydrogen atoms and one oxygen atom have been removed from the peptide bonding process. So, the peptide bonding results in the release of a water molecule…h20. But, we are not finished. More amino acids can link in, and form what is called a polypeptide chain. Some proteins are single polypeptide chains, and other proteins have polypeptide chains linked together. Not all protein contains all 20 of the standard amino acids. Not all protein contains all 20 of the standard amino acids. Proteins are often labeled as complete or incomplete protein. A Complete protein is a protein source that contains a sufficient quantity of all 9 of the essential amino acids that we discussed earlier. An incomplete protein does not contain a sufficient quantity of all 9 of the essential amino acids. Complete protein foods include…animal foods such as red meat, poultry, pork and fish. Eggs and dairy products such as cows milk, yogurt, and cheese. Plant foods such as soy products, black beans, kidney beans, pumpkin seeds, quinoa, pistachios, just to name a few. You can also combine incomplete protein foods to create a complete protein meal. Amino acids also make up most enzymes. These Enzymes are proteins, so they are made by linking amino acids together in a specific and unique order. This chain of amino acids then forms a unique shape that allows the enzyme created to serve a single specific purpose. Enzymes function as catalysts, which means that they speed up the rate at which metabolic processed and reactions occur. Amino acids can also be metabolized for energy. Some hormones like epinephrine, also known as adrenaline, are amino acid derived. Some neurotransmitters like serotonin are derived from amino acids. The amino acid arginine is a precursor of nitric oxide, which helps regulate blood pressure, improves sleep quality and increases endurance and strength. Glutathione, which is a powerful antioxidant is formed from amino acids. Other sources... https://en.wikipedia.org/wiki/Amino_acid http://www.fitday.com/fitness-articles/nutrition/proteins/incomplete-vs-complete-proteins.html http://www.ivyroses.com/HumanBiology/Nutrition/Amino_Acids.php
Views: 47730 Whats Up Dude

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