A chemist carried out an elimination reaction of 1,1-dimethyl-2- (dehydrobromination) bromocyclopentane. The chemist expected the reaction to yield alkene Z as product. However, alkene Z DID NOT form. Instead, three alkenes were produced: one alkene was the major product, the other two alkenes was the minor products. What was the major alkene product that formed? Select one: OA. I B. II C. IV D. III alcohol HEAT 11 Z + (HBr) IV

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(dehydrobromination)
A chemist carried out an elimination reaction
of 1,1-dimethyl-2-
bromocyclopentane. The chemist expected the
reaction to yield alkene Z as product. However,
alkene Z DID NOT form. Instead, three alkenes
were produced: one alkene was the major
product, the other two alkenes was the minor
products.
What was the major alkene product that
formed?
Br
Select one:
A. I
B. II
C. IV
D. III
alcohol
HEAT
||
Z
=
+
(HBr)
IV
Transcribed Image Text:(dehydrobromination) A chemist carried out an elimination reaction of 1,1-dimethyl-2- bromocyclopentane. The chemist expected the reaction to yield alkene Z as product. However, alkene Z DID NOT form. Instead, three alkenes were produced: one alkene was the major product, the other two alkenes was the minor products. What was the major alkene product that formed? Br Select one: A. I B. II C. IV D. III alcohol HEAT || Z = + (HBr) IV
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