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Devise a synthesis of the following compound. You may use HC≡CH, ethylene oxide, and alkyl halides as organic starting materials and any inorganic reagents. Be sure to answer all parts.
CH3CH2CH2CH2CH2CH2C≡CH
Step 1:
A. HC≡CH ---NaH------>
B. HC≡CH ----H2SO4-->
C. HC≡CH ------Br2----->
D. HC≡CH------CH3CH2CH2CH2CH2CH2Br------>

Respuesta :

Answer:

Deprotonation followed by a substitution reaction leads to the formation of given compound.

Explanation:

In the first step, acetylene reacts with sodium hydride to produce a strong nucleophile acetylide anion.

In the second step, acetylide anion gives a substitution nucleophilic bimolecular reaction with 1-bromohexane to produce the given structure.

So a combination of deprotonation and substitution reaction yield the given compound.

Synthesis steps are shown below.

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