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Oksanka [162]
4 years ago
8

Draw all of the constitutional isomeric monochlorination products resulting from the reaction of 2,3−dimethylbutane under radica

l substitution conditions.
(a) primary alkyl halide
(b) tertiary alkyl halide

Chemistry
1 answer:
Elan Coil [88]4 years ago
7 0

Answer:

a) 2-chloro-2,3-dimethylbutane

b) 1-chloro-2,3-dimethylbutane

Explanation:

The <u>monochlorination</u> is a reaction in which we have to add <u>only 1 Cl</u> to the molecule. In this case, we will have to add a Cl to a <u>primary carbon</u> (a) and to a <u>tertiary carbon</u> (b).

In the monochlorination of the primary carbon, we can choose any <u>methyl carbon</u>. For the monochlorination of the terciary carbon we have to choose an <u>CH carbon</u>.

(See the figure)

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NH,F+ _AICI,<br>__NH,CI + __A!F,​
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Explanation:

                          NH₄F+     AICI₃,    →   NH₄CI +   AlF₃

   NH,F: in ionic form

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   AICI in ionic form:

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          NH₄⁺ + Cl⁻ = NH₄Cl

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         Al³⁺ + F⁻   =  AlF₃

                     NH₄F+     AICI₃,    →   NH₄CI +   AlF₃

Now we have to balance the equation with respect to the atoms:

           aNH₄F+     bAICI₃,    →   cNH₄CI +   dAlF₃

  for N: a = c

        H: 4a = 4c

        F:  a = 3d

        Cl: 3b = c

   let a = 1

        c = 1

         b = \frac{1}{3}

        d = \frac{1}{3}

Therefore we can imply that:

     a = 3, b = 1 , c = 3 and d = 1 if we multiply through by 3

          3NH₄F+     AICI₃,    →   3NH₄CI +   AlF₃

Learn more:

Chemical equation brainly.com/question/2924195

#learnwithBrainly

 

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