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:Gramicidin S, a topical antibiotic produced by the bacterium Bacillus brevis, is a cyclic decapeptide formed from five amino acids. Draw the structures of the amino acids that form gramicidin S, and explain why this compound possesses two unusual structural features.

Which of the following amino acids are typically found in the interior of a globular protein, and which are typically found on the surface: (a)phenylalanine; (b)aspartic acid; (c) lysine; (d) isoleucine; (e) arginine; (f) glutamic acid?

Another method to form a peptide bond involves a two-step process:

[1] Conversion of a Boc-protected amino acid to a p-nitrophenyl ester.

[2] Reaction of the p-nitrophenyl ester with an amino acid ester.

  1. Why does a p-nitrophenyl ester “activate” the carboxy group of the first amino acid to amide formation?

  2. Would a p-methoxyphenyl ester perform the same function? Why or why not?

Devise a stepwise synthesis of the tripeptide Val-leu-Val from 3-methylbutanal[CH32CHCH2CHO] as the only organic starting material. You may also use any required inorganic or organic reagents.

What is the predominant form of each of the following amino acids at pH=11? What is the overall charge on the amino acid? (a)valine; (b)proline; (c)glutamic acid; (d)lysine?
See all solutions

Recommended explanations on Chemistry Textbooks

Chemistry Branches

Read Explanation

Kinetics

Read Explanation

Chemical Analysis

Read Explanation

Nuclear Chemistry

Read Explanation

Making Measurements

Read Explanation

Inorganic 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