A product of the hydrogenation of 3,4-dimethyl-3-hexene is shown in the box. Which of the following best describes the product(s) of this reaction? H2 3,4-dimethyl-3-hexene Pd 1 chiral pdt formed 2 chiral pdts formed and they are diastereomers 2 chiral pdts formed and they are enantiomers O 1 achiral meso pdt formed O 1 achiral pdt with no stereocenters formed

A product of the hydrogenation of 3,4-dimethyl-3-hexene is shown in the box. Which of the following best describes the product(s) of this reaction? H2 3,4-dimethyl-3-hexene Pd 1 chiral pdt formed 2 chiral pdts formed and they are diastereomers 2 chiral pdts formed and they are enantiomers O 1 achiral meso pdt formed O 1 achiral pdt with no stereocenters formed

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter16: Aldehydes And Ketones

Section: Chapter Questions

Problem 16.67P: Treatment of -D-glucose with methanol in the presence of an acid catalyst converts it into a mixture...

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Treatment of -D-glucose with methanol in the presence of an acid catalyst converts it into a mixture of two compounds called methyl glucosides (Section 25.3A). In these representations, the six-membered rings are drawn as planar hexagons. (a) Propose a mechanism for this conversion and account for the fact that only the OH on carbon 1 is transformed into an OCH3 group. (b) Draw the more stable chair conformation for each product. (c) Which of the two products has the chair conformation of greater stability? Explain.
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