Log out Go to App
Go to App

Learning Materials

Features

Discover

Chapter 14: Q. 14.64 (page 503)

Draw the condensed structural or line-angle formulas for the products of the following:

a)

b)

c)

Short Answer

Expert verified

Part a)

Part b)

Part c)

Step by step solution

01

step-1 Introduction (Part a)

  • Carboxylic acids are weak acids that neutralize bases by producing hydronium ions in water.
  • The carbon atom of a carbonyl group is bonded to a hydroxyl group to generate a carboxyl group in carboxylic acids.
  • An alkyl or aromatic group might bind to the carboxyl functional group.
02

step-2 given information (part-a)

2-methylethyl propanoate is converted to sodium propanoate by base hydrolysis with NaOH.

03

step-3 Explanation (part-a)

04

step-4  given information (part-b)

Propyl 2-methyl propanoate undergoes acid hydrolysis in this process, yielding 2 -methyl propanoic acid.

05

step-5 Explanation (part-b)

06

step-6  given information (part-c)

Propanamide is hydrolyzed by the base to create sodium propanoate and ammonia in this reaction.

07

step-7 Explanation (part-c)

Unlock Step-by-Step Solutions & Ace Your Exams!

  • Full Textbook Solutions

    Get detailed explanations and key concepts

  • Unlimited Al creation

    Al flashcards, explanations, exams and more...

  • Ads-free access

    To over 500 millions flashcards

  • Money-back guarantee

    We refund you if you fail your exam.

Start your free trial

Over 30 million students worldwide already upgrade their learning with Vaia!

One App. One Place for Learning.

All the tools & learning materials you need for study success - in one app.

Get started for free

Most popular questions from this chapter

Draw the condensed structural or line-angle formula for the ester formed in each of the following reactions:

(a)

(b)

The ester methyl butanoate has the odor and flavor of strawberries. (14.3,14.4)

a. Draw the condensed structural formula for methyl butanoate.

b. Write the IUPAC name for the carboxylic acid and the alcohol used to prepare methyl butanoate.

c. Write the balanced chemical equation for the acid hydrolysis of methyl butanoate.

Identify the compound in each group that is most soluble in water. Explain.

a. propanoic acid, hexanoic acid, benzō̄ic acid

b. pentane, 1-hexanol, propanoic acid

Draw the condensed structural formula for each of the following amides:

a. propionamide

b. 2-methylpentanamide

c. methanamide

d. N,N-dimethyl ethanamide

Write the balanced chemical equation for the dissociation of each of the following carboxylic acids in water:

a. pentanoic acid

b. acetic acid
See all solutions

Recommended explanations on Chemistry Textbooks

Inorganic Chemistry

Read Explanation

Nuclear Chemistry

Read Explanation

Making Measurements

Read Explanation

Organic Chemistry

Read Explanation

The Earths Atmosphere

Read Explanation

Physical Chemistry

Read Explanation
View all explanations

What do you think about this solution?

We value your feedback to improve our textbook solutions.

Study anywhere. Anytime. Across all devices.

Sign-up for free