Log out Go to App
Go to App

Learning Materials

Features

Discover

Chapter 29: Q60. (page 1196)

Draw the organic products formed in each reaction.


Short Answer

Expert verified

Organic synthesis is the formation of organic products using different reagents like DCC, CF3COOHetc.There are numerous organic reactions like esterification, alkylation, and halogenations.

Step by step solution

01

Organic synthesis

Organic synthesis is the formation of organic products using different reagents like DCC, CF3COOHetc.There are numerous organic reactions like esterification, alkylation, and halogenations.

02

Organic products of a, b, and c reactions

1.The organic product of the following reaction is,


b.The organic product of the following reaction is,



c.The organic product of the following reaction is,

03

Organic products of d, e, and f reactions

d.The organic product of the following reaction is,


e.The organic product of the following reaction is,


f.The organic product of the following reaction is,


Formation of organic product

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

Question: Into how many peaks will each proton shown in green be split?

a.

b.

c.

d.

e.

Image Caption

f.

Draw the organic products formed in each reaction.

The enolate derived from diethyl acetamidomalonate is treated with each of the following alkyl halides. After hydrolysis and decarboxylation, what amino acid is formed?

(a)CH3I(b)(CH3)2CHCH2Cl(c)CH3CH2CH(CH3)Br

Write out the steps for the synthesis of each peptide using the Merrifield method:

  1. Ala-Leu-Phe-Phe; (b) Phe-Gly-Ala-Ile.

Propose a structure consistent with each set of data.

a. Compound J: molecular ion at 72; IR peak at 1710 \({\bf{c}}{{\bf{m}}^{{\bf{ - 1}}}}\); \({}^{\bf{1}}{\bf{H}}\)-NMR data (ppm) at 1.0 (triplet, 3 H), 2.1 (singlet, 3 H), and 2.4 (quartet, 2 H)

b. Compound K: molecular ion at 88; IR peak at 3600–3200 \({\bf{c}}{{\bf{m}}^{{\bf{ - 1}}}}\); \({}^{\bf{1}}{\bf{H}}\)-NMR data (ppm) at 0.9 (triplet, 3 H), 1.2 (singlet, 6 H), 1.5 (quartet, 2 H), and 1.6 (singlet, 1 H)
See all solutions

Recommended explanations on Chemistry Textbooks

Physical Chemistry

Read Explanation

Inorganic Chemistry

Read Explanation

Nuclear Chemistry

Read Explanation

Making Measurements

Read Explanation

Organic Chemistry

Read Explanation

The Earths Atmosphere

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