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Chapter 10: Q.12. (page 396)

Question: Draw the products of each elimination reaction.

Short Answer

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Answer

Step by step solution

01

Elimination reactions

In an elimination reaction, any two substituents leave the substrate, leading to the formation of an extra double bond.

02

Products of elimination reaction

The elimination reactions begin with the attack of a nucleophile. The major products of the elimination reaction are the more substituted alkenes.

03

Products of given compounds

Each elimination reaction results in a mixture of alkenes.

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Most popular questions from this chapter

Question: (a) Label the carbon–carbon double bond in A as E or Z. (b) Draw the products (including stereoisomers) formed when A is treated with H2O in the presence of H2SO4.

Question: Draw a stepwise mechanism for the following reaction. Draw the transition state for each step.

Question: How many degrees of unsaturation are present in each compound?

  1. C6H6
  2. role="math" localid="1648637368534" C8H18
  3. C7H8O
  4. C7H11Br
  5. C5H9N

Question: a. What product(s) are formed when the E isomer of C6H5CH=CHC6H5is treated with Br2 , followed by one equivalent of KOH? Label the resulting alkene(s) as E or Z. b. What product(s) are formed when the Z isomer of C6H5CH=CHC6H5 is subjected to the same reaction sequence? c. How are the compounds in parts (a) and (b) related to each other?

Question: Draw a stepwise mechanism for the following reaction.
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