Chemistry, 30.07.2020 04:01, jadkins842
Heating carvone with aqueous sulfuric acid converts it into carvacrol. The mechanism involves the following steps:
1. The terminal alkene of carvone reacts with acid to form tertiary carbocation 1;
2. A hydride shift results in the formation of tertiary carbocation 2;
3. Deprotonation of the ring leads to conjugated diene 3;
4. Deprotonation at the α carbon leads to the product carvacrol.
Required:
Draw the mechanism and then draw the structure of tertiary carbocation 2.
Answers: 1
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The kw for water at 0 °c is 0.12× 10–14 m2. calculate the ph of a neutral aqueous solution at 0 °c.
Answers: 2
Heating carvone with aqueous sulfuric acid converts it into carvacrol. The mechanism involves the fo...
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