2a. The boiling points of hex-1-ene and hex-1-yne are sufficiently close that it is difficult to achieve a clean separation by distillation. Show how you might use the acidity of hex-1-yne to remove the last trace of it from a sample of hex-1- ene. 2b. Predict the products of the following acid-base reactions, or indicate if no reaction would take place. 1. HCC + CH₂OH ii. HCECH + NaOH iii. HC=CNa + H₂C=CH₂ iv. HCECH + CHyLi

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R7P2 Organic Chemistry Problem: Please give as much detail as possible in solving the answer. I do not have an answer key, but any support is appleciated for exam study. Will give a thumbs up regardless. Thanks!

2a. The boiling points of hex-1-ene and hex-1-yne are sufficiently close that it is difficult to achieve a clean separation
by distillation. Show how you might use the acidity of hex-1-yne to remove the last trace of it from a sample of hex-1-
ene.
2b. Predict the products of the following acid-base reactions, or indicate if no reaction would take place.
1. HCEC + CH₂OH
ii. HCECH + NaOH
iii. HCECNa+ H₂C=CH₂
iv. HCECH + CH3L
Transcribed Image Text:2a. The boiling points of hex-1-ene and hex-1-yne are sufficiently close that it is difficult to achieve a clean separation by distillation. Show how you might use the acidity of hex-1-yne to remove the last trace of it from a sample of hex-1- ene. 2b. Predict the products of the following acid-base reactions, or indicate if no reaction would take place. 1. HCEC + CH₂OH ii. HCECH + NaOH iii. HCECNa+ H₂C=CH₂ iv. HCECH + CH3L
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