The cis configuration has the substituted groups on opposite side of the double bond
1 answer:
Answer:
False.
Explanation:
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In this case, according to the attached picture, it is possible for us to evidence that cis- isomers have the substituted groups on the same side of the double bond whereas the trans- isomers have the substituted groups on the opposite side of the double bond.
In such a way, we infer that the given statement is FALSE, because that is the definition for the trans configuration.
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<h2>Heptene formed is -</h2><h2>
</h2>
Explanation:
The two possibilities when the peroxide is not present
-
≡
→
+ HBr →
In presence peroxide,
≡
+ HBr →
- When peroxides are present in the reaction mixture, hydrogen bromide adds to the triple bond of heptane with regioselectivity.
- This reaction is opposite to that of Markovnikov's rule which says that when asymmetrical alkene reacts with a protic acid HX, then the hydrogen of an acid is attached to the carbon with more in number of hydrogen substituents, and the halide (X) group is attached to the carbon with more in number of substituents of alkyl.
- One mole of HBr adds to one mole of 1-heptane.
- The structure of heptene formed is -