Answer all Benzil2. Draw the Newman projection for meso -hydrobenzoin and indicate the absolute configuration about eachchiral, center.3. Give the name of and write the chemical formula for the reducing agent used to convert benzil to benzoin.4. Using chemical equations, account for why anhydrous conditions are required when preparing an alcohol via aGrignard reagent.5. Beginning with benzene, magnesium, and any other reagent show how you would synthesize triphenylmethanol. Use only chemical structures.

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2. Draw the Newman projection for meso -hydrobenzoin and indicate the absolute configuration about each chiral, center.

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter13: Substitution

Section: Chapter Questions

Problem 4E

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Stereochemistry and Isomerism

Stereochemistry deals with the three-dimensional structure and properties of molecules. It explains the arrangement of atoms and their manipulation within a molecule in a 3D structure. Stereochemistry can be dealt with all types of molecules. Based on the stereochemistry of a molecule, the physical and chemical properties of the molecules vary.

Question

Answer all

Benzil
2. Draw the Newman projection for meso -hydrobenzoin and indicate the absolute configuration about each
chiral, center.
3. Give the name of and write the chemical formula for the reducing agent used to convert benzil to benzoin.
4. Using chemical equations, account for why anhydrous conditions are required when preparing an alcohol via a
Grignard reagent.
5. Beginning with benzene, magnesium, and any other reagent show how you would synthesize triphenyl
methanol. Use only chemical structures.

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