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 >
b. hc≡ch -->
c. hc≡ch >
d. hc≡>

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.

increased stability in the completion of fluorine's outer shell.

the answer is 0.8m.

by: nicholas