Draw the structure of the major organic product(s) for the following reaction between an acetylenic anion and an alkyl halide. (The reaction stoichiometry is 1:1.) A carbon carbon triple bond where carbon 1 is a carbanion with a lone pair and carbon 2 is bonded to methyl. This reacts with a 5 carbon chain where carbon 3 has a bromine substituent.

See explanation below

Explanation:

In this case, we are having a reaction between an anion and alkyl halide. The carbon 1 of the anion will act as nucleophile and will attack the electrophile, which is 5 carbon chain with the bromine in the third carbon.

Now, the nucleophyle is an alkyne of 3 carbon. According to the description, it should be:

CH₃ - C ≡ C⁻

And the alkyl halide is:

CH₃ - CH₂ CH(Br) - CH₂ - CH₃

And the final product after the reaction would be the following:

CH₃ - C ≡ C - CH - (CH₂CH₃)₂

However, in the attached picture you can see this better and the mechanism of reaction.

Hope this helps

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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