Chapter 8: Q.20 (page 318)
Which mechanism, E1 or E2, will occur in each reaction?
a.
b.
c.
d.
Short Answer
The products with their mode of reaction are shown below:-
Chapter 8: Q.20 (page 318)
Which mechanism, E1 or E2, will occur in each reaction?
a.
b.
c.
d.
The products with their mode of reaction are shown below:-
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Get started for freeElimination of HBr from 2-bromobutane affords a mixture of but-1-ene and but-2-ene. With sodium ethoxide as base, but-2-ene constitutes 81% of the alkene products, but with potassium tert-butoxide, but-2-ene constitutes only 67% of the alkene products. Offer an explanation for this difference.
Although dehydrohalogenation occurs with anti periplanar geometry, some eliminations have syn periplanar geometry. Examine the starting material and product of each elimination, and state whether the elimination occurs with syn or anti periplanar geometry.
a.
b.
Which alkene in each pair is more stable?
a.
b.
c.
For which double bonds are stereoisomers possible?
a.
b.
c.
What alkenes are formed from each alkyl halide by an E1 reaction? Use the Zaitsev rule to predict the major product.
a.
b.
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