ORGANIC CHEMISTRY-W/STUD.SOLN.MAN.
ORGANIC CHEMISTRY-W/STUD.SOLN.MAN.
10th Edition
ISBN: 9781260001099
Author: Carey
Publisher: MCG
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Chapter 9, Problem 37P

Alkynes undergo hydroboration to give alkenylboranes, which can be oxidized to give carbonyl compounds with hydrogen peroxide. The net result of the two-step sequence is hydration, which gives aldehydes from terminal alkynes.

Chapter 9, Problem 37P, Alkynes undergo hydroboration to give alkenylboranes, which can be oxidized to give carbonyl , example  1

The oxidation step involves an enol intermediate. Using Mechanism 9.1 as a guide, write the structure of the enol that is formed in the conversion of 1-hexyne to hexanal.

Chapter 9, Problem 37P, Alkynes undergo hydroboration to give alkenylboranes, which can be oxidized to give carbonyl , example  2

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1. Base on this experimental results, how do you know that the product which you are turning in is methyl 3-nitrobenzoate(meta substituted product ) rather than either of the other two products?  2. What observation suggests that at least a small amount of one or both of the other two isomers are in the mother liquor?
Explain Huckel's rule.
here is my question can u help me please!

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ORGANIC CHEMISTRY-W/STUD.SOLN.MAN.

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