Draw the structure of the major organic product isolated from the reaction of 1-hexyne with sodium amide in liquid ammonia followed by 1-bromobutane.

CH3(CH2)3CCH --> CH3(CH2)3CCCH2(CH2)2CH3 + NaBr

Explanation:

This reaction are used in the elongation of a terminal alkyne chain, it can be in 2 steps:

Step 1:

NaNH2 is in this reaction is used in the deprotonation of 1-hexyne to give acetylide ions( RCC-). The ion is an nucleophile because of the lone pair of electrons.

Step 2:

This acetylide ion is a basic ion (because 1-hexyne is a weak acid). The alky halide (1-bromobutane) dissociates to form a primary cation and Br- ion. This cation then attacks the acetylide ion, reacts to form carbon-carbon bonds as well as add to carbonyl.

Below is an attachment for the chemical reaction.

for step 7 table c on the lab "newtons law of action"   the average time it took the car to travel .25 meters   was 1.92 seconds.

the average time it took the car to travel 0.50 meters was 2.61 seconds

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