The optical activity of the given form of tartaric acid is to be explained and the structure of its optically active form is to be drawn. Concept introduction: Optically active compounds are those consist of a chiral centre and rotate a plane of polarized light in clockwise and anti-clockwise direction. Tartaric acid is an α -hydroxy- carboxylic acid having a structural formula ( HO 2 CCH ( OH ) CH ( OH ) CO 2 H ) . It also exists in meso form. Meso compounds are those which form superimposable mirror images of each other after having stereogenic centre in its structure. To determine: The explanation for the optical activity of the given form of tartaric acid.
The optical activity of the given form of tartaric acid is to be explained and the structure of its optically active form is to be drawn. Concept introduction: Optically active compounds are those consist of a chiral centre and rotate a plane of polarized light in clockwise and anti-clockwise direction. Tartaric acid is an α -hydroxy- carboxylic acid having a structural formula ( HO 2 CCH ( OH ) CH ( OH ) CO 2 H ) . It also exists in meso form. Meso compounds are those which form superimposable mirror images of each other after having stereogenic centre in its structure. To determine: The explanation for the optical activity of the given form of tartaric acid.
Solution Summary: The author explains that the optical activity of the given form of tartaric acid is explained and the structure of its optically active form is drawn.
Definition Definition Class of organic compounds that contain a carboxyl group ( - COOH ) and has a general formula R - COOH or R - CO 2 H , where R refers to the alkyl, alkenyl, aryl, or other groups. They can undergo different chemical reactions, such as acid-base reactions, esterification, and oxidation. These are essential components of living organisms, playing important roles in metabolic processes, signaling, and as pharmaceuticals.
Chapter 22, Problem 161CP
(a)
Interpretation Introduction
Interpretation: The optical activity of the given form of tartaric acid is to be explained and the structure of its optically active form is to be drawn.
Concept introduction: Optically active compounds are those consist of a chiral centre and rotate a plane of polarized light in clockwise and anti-clockwise direction. Tartaric acid is an
α-hydroxy-carboxylic acid having a structural formula
(HO2CCH(OH)CH(OH)CO2H). It also exists in meso form. Meso compounds are those which form superimposable mirror images of each other after having stereogenic centre in its structure.
To determine: The explanation for the optical activity of the given form of tartaric acid.
(b)
Interpretation Introduction
Interpretation: The optical activity of the given form of tartaric acid is to be explained and the structure of its optically active form is to be drawn.
Concept introduction: Optically active compounds are those consist of a chiral centre and rotate a plane of polarized light in clockwise and anti-clockwise direction. Tartaric acid is an
α-hydroxy-carboxylic acid having a structural formula
(HO2CCH(OH)CH(OH)CO2H). It also exists in meso form. Meso compounds are those which form superimposable mirror images of each other after having stereogenic centre in its structure.
To determine: The structure of the optically active form of tartaric acid.
Predict the major organic product(s) of the following reactions. Indicate which of the following mechanisms is in operation: SN1, SN2, E1, or E2.
(c)
(4pts)
Mechanism:
heat
(E1)
CH3OH
+
1.5pts each
_E1 _ (1pt)
Br
CH3OH
(d)
(4pts)
Mechanism:
SN1
(1pt)
(e)
(3pts)
1111 I
H
10
Ill!!
H
LDA
THF (solvent)
Mechanism: E2
(1pt)
NC
(f)
Bri!!!!!
CH3
NaCN
(3pts)
acetone
Mechanism: SN2
(1pt)
(SN1)
-OCH3
OCH3
1.5pts each
2pts for either product
1pt if incorrect
stereochemistry
H
Br
(g)
“,、
(3pts)
H
CH3OH
+21
Mechanism:
SN2
(1pt)
H
CH3
2pts
1pt if incorrect
stereochemistry
H
2pts
1pt if incorrect
stereochemistry
A mixture of butyl acrylate and 4'-chloropropiophenone has been taken for proton NMR analysis. Based on this proton NMR, determine the relative percentage of each compound in the mixture
Chapter 22 Solutions
WebAssign for Zumdahl/Zumdahl/DeCoste's Chemistry, 10th Edition [Instant Access], Single-Term
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Author:Steven D. Gammon, Ebbing, Darrell Ebbing, Steven D., Darrell; Gammon, Darrell Ebbing; Steven D. Gammon, Darrell D.; Gammon, Ebbing; Steven D. Gammon; Darrell
Author:Steven D. Gammon, Ebbing, Darrell Ebbing, Steven D., Darrell; Gammon, Darrell Ebbing; Steven D. Gammon, Darrell D.; Gammon, Ebbing; Steven D. Gammon; Darrell