10. a) Provide the structures of reagent 1 and 2 that are required to generate the following alkyne: Route 1 Reagent 1 1. NaNH2/NH3 2. CH3Br 2 molar eq HBr H₂ Lindlar's 2 equivalents NaNH, NH3 b) Provide the structure of the product, with the correct stereochemistry where necessary, for each of Catalyst Pd excess Cl₂ Route 2 NaNH, NH3 Reagent 2 the following transformations involving alkynes. If there is no reaction, write 'NR' in the respective box.
10. a) Provide the structures of reagent 1 and 2 that are required to generate the following alkyne: Route 1 Reagent 1 1. NaNH2/NH3 2. CH3Br 2 molar eq HBr H₂ Lindlar's 2 equivalents NaNH, NH3 b) Provide the structure of the product, with the correct stereochemistry where necessary, for each of Catalyst Pd excess Cl₂ Route 2 NaNH, NH3 Reagent 2 the following transformations involving alkynes. If there is no reaction, write 'NR' in the respective box.
Chemistry
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ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
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Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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
Transcribed Image Text:10. a) Provide the structures of reagent 1 and 2 that are required to generate the following alkyne:
Route 1
Reagent 1
1. NaNH2/NH3
2. CH3Br
2 molar eq
HBr
H₂
Lindlar's
2 equivalents
NaNH,
NH3
b) Provide the structure of the product, with the correct stereochemistry where necessary, for each of
Catalyst
Pd
excess
Cl₂
Route 2
NaNH,
NH3
Reagent 2
the following transformations involving alkynes. If there is no reaction, write 'NR' in the
respective box.
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