Organic Chemistry
4th Edition
ISBN: 9780073402772
Author: Janice G. Smith
Publisher: MCG
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Question
Chapter 3, Problem 3.52P
Interpretation Introduction
(a)
Interpretation: To identify the number of amide
Concept introduction: A functional group is an atom or a molecule in the compound which gives the characteristic property to that particular compound. It is the site where the reaction takes place.
Interpretation Introduction
(b)
Interpretation: To identify which OH groups are attached to sp3 C-atom and which are attached at sp2 hybridized C-atoms.
Concept introduction: A sp3 hybridization is shown by the C-atoms which are bonded to four substituents and a sp2 carbon atom is bonded to three substituents.
Interpretation Introduction
(c)
Interpretation: To identify whether the given compound vancomycin is water soluble or not.
Concept introduction: Hydrogen bonding is seen in those molecules in which a hydrogen atom is bonded to an electronegative atom containing a lone pair like F, N or O. Hydrogen bond is formed when a H atom bonded to the electronegative atom gets attracted towards the lone pair of the electronegative atom present on another molecule. Thus, a molecule can form hydrogen bond with water if it contains electronegative atoms like F, N or O.
Interpretation Introduction
(d)
Interpretation: To identify the most acidic proton.
Concept introduction: The most acidic proton is the one present on the functional group which can donate a proton readily and can form salt.
Interpretation Introduction
(e)
Interpretation: To identify three functional groups which can form hydrogen bonds.
Concept introduction: Hydrogen bonding is seen in those molecules in which a hydrogen atom is bonded to an electronegative atom containing a lone pair like F, N or O. Hydrogen bond is formed when a H atom bonded to the electronegative atom gets attracted towards the lone pair of the electronegative atom present on another molecule.
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Students have asked these similar questions
Predict the approximate size of the following bond angles.
a. the C-O-C bond angle in an ether b. the C-N-C bond angle in a secondary amine c. the C-O-H bond angle in an alcohol d. the C-N-C bond angle in a quaternary ammonium salt
3. In the structure of Lisinopril below, Identify the main functional group in the molecule?
NH2
G
HO
14
5
H
H
16
8
ZH
10 11
N
H
18
19
OH
A. Aromatic ring-Carboxyl group-Amino group
B. Only the Aromatic and Amide group is there.
C. Ester Group Only.
B. Aromatic ring-Carboxyl group-Amino group-Amide group.
1. what priority functional group of ff organic compound?
a. carboxyl
b. hydroxide
c. hydroxyl
d. carbonyl
2. what group does the ff organic compound belong?
a. azo
b. diazo
c. aromatic
d. organosulfur
3. what group does the ff organic compound belong?
a. azo
b. amines
c. diazo
d. nitriles
Chapter 3 Solutions
Organic Chemistry
Ch. 3 - Prob. 3.1PCh. 3 - Prob. 3.2PCh. 3 - Draw the structure of a compound fitting each...Ch. 3 - Draw structures that fit each description and name...Ch. 3 - What types of intermolecular forces are present in...Ch. 3 - Prob. 3.6PCh. 3 - Explain why the boiling point of propanamide, is...Ch. 3 - Predict which compound in each pair has the higher...Ch. 3 - Prob. 3.9PCh. 3 - Prob. 3.10P
Ch. 3 - a Label the hydrophobic and hydrophilic portions...Ch. 3 - Prob. 3.12PCh. 3 - Prob. 3.13PCh. 3 - Prob. 3.14PCh. 3 - Prob. 3.15PCh. 3 - Nonactin and valinomycin each contain only two...Ch. 3 - Prob. 3.17PCh. 3 - Problem 3.26 Label the electrophilic and...Ch. 3 - Problem 3.27 Considering only electron density,...Ch. 3 - The fact that sweet-tasting carbohydrates like...Ch. 3 - 3.29
Identify the functional groups in the...Ch. 3 - Prob. 3.22PCh. 3 - 3.32 Identify the functional groups in each...Ch. 3 - Draw the seven constitutional isomers having...Ch. 3 - 3.33 Identify each functional group located in the...Ch. 3 - Draw seven constitutional isomers with molecular...Ch. 3 - Prob. 3.27PCh. 3 - Prob. 3.28PCh. 3 - Prob. 3.29PCh. 3 - Intramolecular force of attraction are often...Ch. 3 - 3.40 (a) Draw four compounds with molecular...Ch. 3 - Prob. 3.32PCh. 3 - Explain why CH3CH2NHCH3 has higher boiling point...Ch. 3 - Prob. 3.34PCh. 3 - Prob. 3.35PCh. 3 - Explain the observed trend in the melting points...Ch. 3 - Prob. 3.37PCh. 3 - Prob. 3.38PCh. 3 - Prob. 3.39PCh. 3 - 3.48 Explain why diethylether and have similar...Ch. 3 - Prob. 3.41PCh. 3 - 3.50 Predict the solubility of each of the...Ch. 3 - Prob. 3.43PCh. 3 - Prob. 3.44PCh. 3 - THC is the active component in marijuana, and...Ch. 3 - Prob. 3.46PCh. 3 - Prob. 3.47PCh. 3 - Prob. 3.48PCh. 3 - Label the electrophilic and nucleophilic sites in...Ch. 3 - By using only electron density arguments,...Ch. 3 - Prob. 3.51PCh. 3 - Prob. 3.52PCh. 3 - Prob. 3.53PCh. 3 - Prob. 3.54PCh. 3 - Prob. 3.55PCh. 3 - Recall from section 1.10B that there is restricted...
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