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The chlorination of pentane gives a mixture of three monochlorinated products.

(a) Draw their structures.

(b) Predict the ratios in which these monochlorination products will be formed, remembering that a chlorine atom abstracts a secondary hydrogen about 4.5 times as fast as it abstracts a primary hydrogen.

Short Answer

Expert verified

(a)

(b) Ratio of the products are 18.18% : 54.54% : 27.27%.

Step by step solution

01

Primary hydrogen (1o)

A primary hydrogen may be defined as a hydrogen on a carbon attached to only one other carbon atom.

02

Secondary hydrogen (2o)

A secondary hydrogen may be defined as a hydrogen on a carbon attached to only two other carbon atoms.

03

Tertiary hydrogen (3o)

A tertiary hydrogen may be defined as a hydrogen on a carbon attached to three other carbon atoms.

04

Structures of three monochlorinated product and the ratios in which they are formed.

a)

Three monochlorinated products formed are, , and.

(b)

In case of 1- chloropentane,

(6 primary hydrogen) x (reactivity 1.0) =6.0 relative amount of reaction.

In case of 2-chloropentane,

(4 primary hydrogen) x (reactivity 4.5) =18 relative amount of reaction.

In case of 3-chloropentane,

(2 primary hydrogen) x (reactivity 4.5) = 9.0 relative amount of reaction.

Now,

Fraction of 1-chloropentane =6.0/ 6.0+18+9.0 = (6.0/33) x 100% =18.18%.

Fraction of 2-chloropentane =18/ 6.0+18+9.0 = (18/33) x 100% =54.54%.

Fraction of 3-chloropentane =9.0/ 6.0+18+9.0 = (9.0/33) x 100% =27.27%.

Hence, ratio of the products is 18.18% : 54.54% : 27.27%.

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Most popular questions from this chapter

Question: (a) Use bond-dissociation enthalpies from Table 4-2 (page 203), calculate the heat of reaction for each step in the free-radical bromination of methane.

(b) Calculate the overall heat of reaction.

2,3-Dimethylbutanereacts with bromine in the presence of light to give a mono brominate product. Further reaction gives a good yield of a dibrominated product. Predict the structures of these products, and propose a mechanism for the formation of the monobrominated product.

(a) When n-heptaneburns in a gasoline engine, the combustion process takes place too quickly. The explosive detonation makes a noise called knocking. When 2,2,4 trimethylpentane (isooctane) is burned, combustion takes place in a slower, more controlled manner. Combustion is a free-radical chain reaction, and its rate depends on the reactivity of the free-radical intermediates. Explain why isooctane has less tendency to knock than doesn-heptane

(b) Alkoxy radicals (R-O)are generally more stable than alkyl (R) radicals. Write an equation showing an alkyl free radical (from burning gasoline) abstracting a hydrogen atom from tert-butyl alcohol,(CH3)3COH. Explain whytert-butyl alcohol works as an antiknock additive for gasoline.

(c) Use the information in Table 4-2 (page 203) to explain why toluene (PhCH3) has a very high-octane rating of 111. Write an equation to show how toluene reacts with an alkyl free radical to give a relatively stable radical.

Under certain conditions, the bromination of cyclohexene follows an unusual rate law:

(a) What is the kinetic order with respect to cyclohexene?

(b) What is the kinetic order with respect to bromine?

(c) What is the kinetic order overall?

For each compound, predict the major product of free-radical bromination. Remember that bromination is highly selective, and only the most stable radical will be formed.

(a) cyclohexane

(b) methylcyclopentane

(c) decalin

(d) hexane

(e)

(f)

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