Draw the product formed when the following diene is treated with one equivalent of HCl. Do not show stereochemistry in your answ
er.
1 answer:
Answer:
4-chloro-4-methyl-cyclohexene.
Explanation:
Hello,
On the attached picture you will find the chemical reaction forming the required product, 4-chloro-4-methyl-cyclohexene. In this case, according to the Markovnicov’s rule, it is more likely for the chlorine to be substituted at the carbon containing the methyl radical in addition to the hydrogen to the next carbon to break the double bond and yield the presented product.
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Answer:
cis 2,3-dibromo- 2-butene
trans 2,3-dibromo- 2-butene
Explanation:
The cis-trans or geometric isomerism is due to restricted rotation around a carbon-carbon bond. This restriction may be due to the presence of double bonds or cycles.
The carbon-carbon double bond prevents free rotation of atoms in molecules. These two molecules have the same atoms, but they are different molecules. They are geometric isomers to each other.
The given compound can exist in the form of two isomers, cis and trans. The isomer that has the substituents on the same side is called cis, and the one that has them on opposite sides is trans.
