(1) KNH, NH, [2] H20 but-2-yne but-1-yne [1] KNH2, NH, Г2] Н.о 2,5-dimethylhex-3-yne 2,5-dimethylhexa-2,3-diene

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Chapter1: Chemical Foundations
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Write a stepwise mechanism for each of the following reactions. Explain why a more stable alkyne (but-2-yne) is isomerized to a less stable alkyne (but-1-yne), but under similar conditions. 2.5-dimethylhex-3-yne forms 2,5-dimethylhexa-2.3-diene.

(1) KNH, NH,
[2] H20
but-2-yne
but-1-yne
[1] KNH2, NH,
Г2] Н.о
2,5-dimethylhex-3-yne
2,5-dimethylhexa-2,3-diene
Transcribed Image Text:(1) KNH, NH, [2] H20 but-2-yne but-1-yne [1] KNH2, NH, Г2] Н.о 2,5-dimethylhex-3-yne 2,5-dimethylhexa-2,3-diene
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