(a)
Interpretation:
The structure of two possible products formed by hydrogenation of linolenic acid with one equivalent H2 in the presence of Pd catalyst should be drawn.
Concept Introduction:
Lipids are
(b)
Interpretation:
The structure of the productformed from complete hydrogenation of linolenic acid should be determined.
Concept Introduction:
Lipids are biomolecules that are involved in different biochemical reactions. They are special types of organic molecules that can only identify with the help of their physical properties and not by the presence of any certain functional group. In general, lipids contain a large number of C-C and C-H bonds with few polar functional groups such as −OH, -SH, etc.For example, triacylglycerol consists of three ester groups, whereas, Vitamin E is composed of both ether and phenolic groups.
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CONNECT IA GENERAL ORGANIC&BIO CHEMISTRY
- When the conjugate acid of aniline, C6H5NH3+, reacts with the acetate ion, the following reaction takes place: C6H5NH3+(aq)+CH3COO(aq)C6H5NH2(aq)+CH3COOH(aq) If Kafor C6H5NH3+ is 1.35105 and Kafor CH3COOH is 1.86105 , what is K for the reaction?arrow_forwardDraw the principal organic reactants, reagents, or products of the following reactions. Fill out the blank, for products, draw all major products showing stereo isomers, if present.arrow_forwardDraw structures corresponding to the following IUPAC names: (d) 4-Ethyl-2-propyloctanoic acid (e) 2-Cyclobutenecarbonitrilearrow_forward
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- Alkenes can be converted to alcohols by reaction with mercuric acetate to form a β-hydroxyalkylmercury(II) acetate compound, a reaction called oxymercuration. Subsequent reduction with NaBH4 reduces the C–Hg bond to a C–H bond, forming the alkyl alcohol, a reaction called demercuration. Draw the structures of the Hg-containing compound(s) and the final alcohol product(s) formed in the following reaction sequence, omitting byproducts. If applicable, draw hydrogen at a chirality center and indicate stereochemistry via wedge-and-dash bonds.arrow_forwardAlkenes can be converted to alcohols by reaction with mercuric acetate to form a β-hydroxyalkylmercury(II) acetate compound, a reaction called oxymercuration. Subsequent reduction with NaBH4 reduces the C–Hg bond to a C–H bond, forming the alkyl alcohol, a reaction called demercuration. Draw the structures of the Hg-containing compound(s) and the final alcohol product(s) formed in the following reaction sequence, omitting byproducts. If applicable, draw hydrogen at a chirality center and indicate stereochemistry via wedge-and-dash bonds.arrow_forwardname the alcohol which will be oxidised by Br2/KOH ? if any (a) methanol (b) ethanol (c) propanolarrow_forward
- Chemistry: Principles and PracticeChemistryISBN:9780534420123Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward MercerPublisher:Cengage LearningChemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage Learning