CONNECT IA GENERAL ORGANIC&BIO CHEMISTRY
CONNECT IA GENERAL ORGANIC&BIO CHEMISTRY
4th Edition
ISBN: 9781260562620
Author: SMITH
Publisher: MCG
Question
Book Icon
Chapter 18.2, Problem 18.4P
Interpretation Introduction

(a)

Interpretation:

The structure corresponding to N-methylaniline is to be drawn.

Concept Introduction:

  • Amines are organic compounds which are derived from ammonia by replacing one or more hydrogen atoms of ammonia by the alkyl groups. The amines can be classified as-
  1. Primary amines ( RNH2 ) - When one hydrogen of ammonia is replaced by the alkyl or aryl group.
  2. Secondary amines ( R2NH ) - When two hydrogen atoms of ammonia are replaced by the alkyl or aryl groups.
  3. Tertiary amine ( R3N ) - When all three hydrogen atoms of ammonia are replaced by the alkyl or aryl groups.

Interpretation Introduction

(b)

Interpretation:

The structure corresponding to m-Ethylaniline is to be drawn.

Concept Introduction:

  • Amines are organic compounds which are derived from ammonia by replacing one or more hydrogen atoms of ammonia by the alkyl groups. The amines can be classified as-
  1. Primary amines ( RNH2 ) - When one hydrogen of ammonia is replaced by the alkyl or aryl group.
  2. Secondary amines ( R2NH) - When two hydrogen atoms of ammonia are replaced by the alkyl or aryl groups.
  3. Tertiary amine ( R3N) - When all three hydrogen atoms of ammonia are replaced by the alkyl or aryl groups.

Interpretation Introduction

(c)

Interpretation:

The structure corresponding to 3,5-diethylaniline is to be drawn.

Concept Introduction:

  • Amines are organic compound which are derived from ammonia by replacing one or more hydrogen atoms of ammonia by the alkyl groups. The amines can be classified as-
  1. Primary amines ( RNH2 ) - When one hydrogen of ammonia is replaced by the alkyl or aryl group.
  2. Secondary amines ( R2NH ) - When two hydrogen atoms of ammonia are replaced by the alkyl or aryl groups.
  3. Tertiary amine ( R3N ) - When all three hydrogen atoms of ammonia are replaced by the alkyl or aryl groups.

Interpretation Introduction

(d)

Interpretation:

The structure corresponding to N,N-diethylaniline is to be drawn.

Concept Introduction:

  • Amines are organic compound which are derived from ammonia by replacing one or more hydrogen atoms of ammonia by the alkyl groups. The amines can be classified as-
  1. Primary amines ( RNH2 ) - When one hydrogen of ammonia is replaced by the alkyl or aryl group.
  2. Secondary amines ( R2NH ) - When two hydrogen atoms of ammonia are replaced by the alkyl or aryl groups.
  3. Tertiary amine ( R3N ) - When all three hydrogen atoms of ammonia are replaced by the alkyl or aryl groups.

Blurred answer
Students have asked these similar questions
Problem 5-48 Assign R or S configurations to the chirality centers in ascorbic acid (vitamin C). OH H OH HO CH2OH Ascorbic acid O H Problem 5-49 Assign R or S stereochemistry to the chirality centers in the following Newman projections: H Cl H CH3 H3C. OH H3C (a) H H H3C (b) CH3 H Problem 5-52 Draw the meso form of each of the following molecules, and indicate the plane of symmetry in each: OH OH (a) CH3CHCH2CH2CHCH3 CH3 H3C. -OH (c) H3C CH3 (b) Problem 5-66 Assign R or S configurations to the chiral centers in cephalexin, trade-named Keflex, the most widely prescribed antibiotic in the United States. H2N H IHH S Cephalexin N. CH3 CO₂H
Steps and explanationn please.
Steps and explanationn please.

Chapter 18 Solutions

CONNECT IA GENERAL ORGANIC&BIO CHEMISTRY

Ch. 18.5 - Prob. 18.8PCh. 18.5 - Naloxone is a drug used to treat overdoses of...Ch. 18.6 - Prob. 18.4PPCh. 18.6 - Prob. 18.10PCh. 18.6 - Prob. 18.11PCh. 18.6 - Name each ammonium salt. a. ( CH3 NH3)+Cl b. [( CH...Ch. 18.6 - Prob. 18.6PPCh. 18.6 - Prob. 18.12PCh. 18.7 - Prob. 18.13PCh. 18.7 - Prob. 18.14PCh. 18.8 - Prob. 18.15PCh. 18.8 - Prob. 18.16PCh. 18.8 - Prob. 18.17PCh. 18.8 - Prob. 18.18PCh. 18.9 - Prob. 18.19PCh. 18.9 - Prob. 18.20PCh. 18.9 - Prob. 18.21PCh. 18.10 - Prob. 18.22PCh. 18 - Prob. 23PCh. 18 - Prob. 24PCh. 18 - Prob. 25PCh. 18 - Prob. 26PCh. 18 - Prob. 27PCh. 18 - Prob. 28PCh. 18 - Prob. 29PCh. 18 - Prob. 30PCh. 18 - Prob. 31PCh. 18 - Prob. 32PCh. 18 - Give an acceptable name for each amine. a. b.Ch. 18 - Give an acceptable name for each amine. a. b.Ch. 18 - Give an acceptable name for each amine. a. b. c....Ch. 18 - Give an acceptable name for each amine. a. CH3(...Ch. 18 - Prob. 37PCh. 18 - Prob. 38PCh. 18 - Prob. 39PCh. 18 - Prob. 40PCh. 18 - Prob. 41PCh. 18 - Prob. 42PCh. 18 - Prob. 43PCh. 18 - Prob. 44PCh. 18 - Which compound in each pair has the higher boiling...Ch. 18 - Which compound in each pair has the higher boiling...Ch. 18 - Draw the hydrogen-bonding interactions that occur...Ch. 18 - Prob. 48PCh. 18 - Prob. 49PCh. 18 - Which compound has the higher water solubility:...Ch. 18 - Prob. 51PCh. 18 - Prob. 52PCh. 18 - Draw the products of each acid-base reaction. a....Ch. 18 - Draw the products of each acid-base reaction. a....Ch. 18 - Prob. 55PCh. 18 - Prob. 56PCh. 18 - What type of nitrogen heterocycle occurs in both...Ch. 18 - Only one of the N atoms in nicotine has a trigonal...Ch. 18 - Prob. 59PCh. 18 - Prob. 60PCh. 18 - Why are aqueous solutions of an alkaloid slightly...Ch. 18 - Prob. 62PCh. 18 - Prob. 63PCh. 18 - Explain why patients with Parkinson’s disease...Ch. 18 - Prob. 65PCh. 18 - Prob. 66PCh. 18 - Prob. 67PCh. 18 - Prob. 68PCh. 18 - Locate the atoms of 2-phenylethylamine in the...Ch. 18 - Locate the atoms of 2-phenylethylamine in the...Ch. 18 - Give an example of an antihistamine. Explain how...Ch. 18 - Give an example of an anti-ulcer drug, and explain...Ch. 18 - Prob. 73PCh. 18 - Prob. 74PCh. 18 - Prob. 75PCh. 18 - Prob. 76PCh. 18 - Prob. 77PCh. 18 - Prob. 78PCh. 18 - Prob. 79PCh. 18 - Why do some antihistamines cause drowsiness while...Ch. 18 - Prob. 81PCh. 18 - Prob. 82PCh. 18 - Compare the structures of morphine and heroin....Ch. 18 - Prob. 84CP
Knowledge Booster
Background pattern image
Similar questions
Recommended textbooks for you
Text book image
Chemistry for Today: General, Organic, and Bioche...
Chemistry
ISBN:9781305960060
Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen
Publisher:Cengage Learning