Organic Chemistry

4th Edition

ISBN: 9780077479824

Author: SMITH, Janice Gorzynski/

Publisher: McGraw-Hill College

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Textbook Question

Chapter 11, Problem 11.68P

Explain why an optically active solution of ( R ) − α − methylbutyrophenone loses its optical activity when dilute acid is added to the solution.

Chapter 11, Problem 11.68P, 11.65 Explain why an optically active solution of loses its optical activity when dilute acid is

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Chapter 11, Problem 11.67P

Chapter 12, Problem 12.1P

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Explain why a base can remove a proton from the alpha-carbon of N,N-dimethylethanamide but not from the alpha-carbon of either N-methylethanamide or ethanamide.

Explain why a base can remove a proton from the a-carbon of N,N-dimethylethanamide but not from the α-carbon of either N-methylethanamide or ethanamide.

Explain why a proton can be removed from the 'alpha-carbon of N,N-dimethylethanamide but not from the alpha-carbon of either N-methylethanamide or ethanamide.

Chapter 11 Solutions

Organic Chemistry

Ch. 11 - Draw structures for the three alkynes having...Ch. 11 - Prob. 11.2P Ch. 11 - Give the IUPAC name for each compound.Ch. 11 - Give the structures corresponding to each of the...Ch. 11 - Prob. 11.5P Ch. 11 - Prob. 11.6P Ch. 11 - Which bases can deprotonate acetylene? The pKa...Ch. 11 - Draw the organic products formed when each alkyne...Ch. 11 - Prob. 11.9P Ch. 11 - Problem 11.9 Draw the products formed when is...

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