EP ORGANIC CHEMISTRY-OWL V2 ACCESS
EP ORGANIC CHEMISTRY-OWL V2 ACCESS
8th Edition
ISBN: 9781305582453
Author: Brown
Publisher: Cengage Learning
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Chapter 7.9, Problem 7.6P

(a)

Interpretation Introduction

Interpretation:

1-Heptanol is synthesised using given synthetic scheme has to be shown.

Concept introduction:

The Lindlar catalyst is a deactivated hydrogenation catalyst that stops alkyne hydrogenation at the alkene stage, allowing conversion of alkynes to cis-alkenes. Hydroboration followed by an acid workup (instead of basic peroxide) also gives cis-alkenes from alkynes. Hydroboration–protonolysis is an alternative way to prepare a cis-alkene from an alkyne.

Hydroboration–protonolysis is an alternative way to prepare a cis-alkene from an alkyne.

(b)

Interpretation Introduction

Interpretation:

2-Heptanol is synthesised using given synthetic scheme has to be shown.

Concept introduction:

The Lindlar catalyst is a deactivated hydrogenation catalyst that stops alkyne hydrogenation at the alkene stage, allowing conversion of alkynes to cis-alkenes. Hydroboration followed by an acid workup (instead of basic peroxide) also gives cis-alkenes from alkynes. Hydroboration–protonolysis is an alternative way to prepare a cis-alkene from an alkyne.

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Use the Henderson-Hasselbalch equation to calculate pH of a buffer containing 0.050M benzoic acidand 0.150M sodium benzoate. The Ka of benzoic acid is 6.5 x 10-5
A. Draw the structure of each of the following alcohols. Then draw and name the product you would expect to produce by the oxidation of each. a. 4-Methyl-2-heptanol b. 3,4-Dimethyl-1-pentanol c. 4-Ethyl-2-heptanol d. 5,7-Dichloro-3-heptanol
What is the pH of a 1.0 L buffer made with 0.300 mol of HF (Ka = 6.8 × 10⁻⁴) and 0.200 mol of NaF to which 0.160 mol of NaOH were added?

Chapter 7 Solutions

EP ORGANIC CHEMISTRY-OWL V2 ACCESS

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