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tigry1 [53]
3 years ago
9

Consider the given structure of the product of a Diels-Alder reaction. Ring made up of six carbons with a double bond between ca

rbons 1 and 2 and a chlorine on both carbons 4 and 5. The two chlorines are on the same side of the ring. What reactants are necessary to make the product
Chemistry
1 answer:
Anni [7]3 years ago
6 0

Answer:

See explanation below

Explanation:

First of all, a Diels Alder reaction is very useful to synthetize rings of 6 carbons. In order to do this, we need two reactants. A dienophile and a conjugate diene.

The conjugate diene, is usually a 4 or 5 carbons, with two double bonds, both conjugate and the dienophile, usually have one double bond and an withdrawing atractor group on 1 carbon.

We already have the product here, which is a ring of 6 carbons, with a double bond and chlorine in two carbons. The only way to do this is putting a conjugate diene of 4 carbons, and a dienophile with 3 carbons and 2 chlorines.

The mechanism of reaction is in the attached picture.

Hope this helps

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Here we have to draw the four isomers of the compound 3-bromo-4-fluorohexane.

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The four different isomers as shown in the figure are 3R-, 4R-; 3S-, 4S; 3R, 4S and 3S-, 4R- 3-bromo-4-fluorohexane.

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