Question 2

Chemistry

1 answer:

Thepotemich [5.8K]2 years ago

3 0

Answer:

1-Pentene

Explanation:

If we look at all the options listed, we will notice that the rate of reaction of bromine with each one differs significantly.

For 1-pentene, addition of bromine across the double bond is a relatively fast process. It is usually used as a test for unsaturation. Bromine water is easily decolorized by alkenes.

Cyclohexane, heptane are alkanes. They can only react with chlorine in the presence of sunlight. This is a substitution reaction. It does not occur easily. A certain quantum of light is required for the reaction to occur.

For benzene, bromine can only react with it by electrophilic substitution in which the benzene ring is retained. A Lewis acid is often required for the reaction to occur and it doesn't occur easily.

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5-Methyl-5-ethyldecane should be the answer .

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2 years ago

Is each of the following statements true or false? Correct any that are false.

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5 months ago

Construct a three-step synthesis of trans-2-pentene from acetylene by dragging the appropriate formulas into the bins. Note that

adelina 88 [10]

Answer:

The three-step synthesis of trans-2-pentene from acetylene is as follows.

<u>Step -1:</u> Formation of higher order terminal alkyne on reaction with sodium acetylides with haloalkanes.

<u>Step -2:</u> Formation terminal alkyne to nonterminal alkynes.

<u>Step -3:</u> Formation of trans-pent - 2-pent-ene by reduction.

Explanation:

Synthesis of trans-pent-2-yne from ethyne takes place is mainly a three step synthesis which involves formation of higher order terminal alkyne on reaction with sodium acetylides with haloalkane. Second step involves the further alkylation of terminal alkynes to higher order nonterminal alkynes and the third step involves the formation of trans-2-ene by dissolving reduction method.

The chemical reaction of each step of chemical reactions is as follows.