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Emil Fischer synthesized L-gulose, an unusual aldohexose

Organic Chemistry | 8th Edition | ISBN: 9780321768414 | Authors: L.G. Wade Jr ISBN: 9780321768414 33

Solution for problem 20P Chapter 23

Organic Chemistry | 8th Edition

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Organic Chemistry | 8th Edition | ISBN: 9780321768414 | Authors: L.G. Wade Jr

Organic Chemistry | 8th Edition

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Problem 20P

Emil Fischer synthesized L-gulose, an unusual aldohexose that reduces to give D-glucitol. Suggest a structure for this L sugar, and show how L-gulose gives the same alditol as D-glucose. (Hint: D-Glucitol has –CH2OH groups at both ends. Either of these primary alcohol groups might have come from reduction of an aldehyde.)

Step-by-Step Solution:

Solution 20P

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Chapter 23, Problem 20P is Solved
Textbook: Organic Chemistry
Edition: 8
Author: L.G. Wade Jr
ISBN: 9780321768414

This textbook survival guide was created for the textbook: Organic Chemistry, edition: 8. The full step-by-step solution to problem: 20P from chapter: 23 was answered by , our top Chemistry solution expert on 05/06/17, 06:41PM. This full solution covers the following key subjects: groups, gulose, glucitol, alcohol, both. This expansive textbook survival guide covers 25 chapters, and 1336 solutions. Since the solution to 20P from 23 chapter was answered, more than 257 students have viewed the full step-by-step answer. Organic Chemistry was written by and is associated to the ISBN: 9780321768414. The answer to “Emil Fischer synthesized L-gulose, an unusual aldohexose that reduces to give D-glucitol. Suggest a structure for this L sugar, and show how L-gulose gives the same alditol as D-glucose. (Hint: D-Glucitol has –CH2OH groups at both ends. Either of these primary alcohol groups might have come from reduction of an aldehyde.)” is broken down into a number of easy to follow steps, and 51 words.

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Emil Fischer synthesized L-gulose, an unusual aldohexose

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