Glycine not being an optically active compound is to be explained. Concept introduction: Amino acids are defined as organic compounds which contain amine ( -NH 2 ) and carboxyl ( -COOH ) functional groups , along with a side chain (R group) attached to each amino acid. Glycine is an amino acid that consists of a single hydrogen atom in its side chain with a molecular formula of NH 2 CH 2 COOH . Optically active compounds are those consist of a chiral centre and rotate a plane of polarized light in clockwise and anti-clockwise direction. To determine: The explanation of glycine for not having an optically active compound.
Glycine not being an optically active compound is to be explained. Concept introduction: Amino acids are defined as organic compounds which contain amine ( -NH 2 ) and carboxyl ( -COOH ) functional groups , along with a side chain (R group) attached to each amino acid. Glycine is an amino acid that consists of a single hydrogen atom in its side chain with a molecular formula of NH 2 CH 2 COOH . Optically active compounds are those consist of a chiral centre and rotate a plane of polarized light in clockwise and anti-clockwise direction. To determine: The explanation of glycine for not having an optically active compound.
Solution Summary: The author explains that glycine is not optically active due to the absence of a chiral carbon in its structure.
Definition Definition Group of atoms that shape the chemical characteristics of a molecule. The behavior of a functional group is uniform in undergoing comparable chemical reactions, regardless of the other constituents of the molecule. Functional groups aid in the classification and anticipation of reactivity of organic molecules.
Chapter 22, Problem 110E
Interpretation Introduction
Interpretation: Glycine not being an optically active compound is to be explained.
Concept introduction: Amino acids are defined as organic compounds which contain amine(-NH2) and carboxyl
(-COOH)functional groups, along with a side chain (R group) attached to each amino acid. Glycine is an amino acid that consists of a single hydrogen atom in its side chain with a molecular formula of
NH2CH2COOH. Optically active compounds are those consist of a chiral centre and rotate a plane of polarized light in clockwise and anti-clockwise direction.
To determine: The explanation of glycine for not having an optically active compound.
Fill in the blanks by selecting the appropriate term from below:
For a process that is non-spontaneous and that favors products at equilibrium, we know that a) ΔrG∘ΔrG∘ _________, b) ΔunivSΔunivS _________, c) ΔsysSΔsysS _________, and d) ΔrH∘ΔrH∘ _________.
Highest occupied molecular orbital
Lowest unoccupied molecular orbital
Label all nodes and regions of highest and lowest electron density for both orbitals.
Relative Intensity
Part VI. consider the multi-step reaction below for compounds A, B, and C.
These compounds were subjected to mass spectrometric analysis and
the following spectra for A, B, and C was obtained.
Draw the structure of B and C and match all three compounds
to the correct spectra.
Relative Intensity
Relative Intensity
20
NaоH
0103
Br
(B)
H2504
→ (c)
(A)
100-
MS-NU-0547
80
40
20
31
10
20
100-
MS2016-05353CM
80
60
100
MS-NJ-09-3
80
60
40
20
45
J.L
80
S1
84
M+
absent
राग
135 137
S2
62
164 166
11
S3
25
50
75
100
125
150
175
m/z