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Ch.10 - Structure and Synthesis of Alcohols
Wade - Organic Chemistry 9th Edition
Wade9th EditionOrganic ChemistryISBN: 9780135213728Non è quello che usi tu?Cambia libro di testo
Capitolo 10, Problema 56b

Often, compounds can be synthesized by more than one method. Show how this 3° alcohol can be made from the following:
Structural formula of a tertiary alcohol with an -OH group, illustrating synthesis from two different alkenes.
(b) two different alkenes

Guida verificata passo dopo passo
1
Step 1: Identify the target molecule as a tertiary alcohol (3° alcohol) with the hydroxyl group (-OH) attached to a carbon that is bonded to three other carbon atoms.
Step 2: Recognize that tertiary alcohols can be synthesized via the acid-catalyzed hydration of alkenes or hydroboration-oxidation reactions. The key is to select alkenes that will lead to the correct placement of the hydroxyl group.
Step 3: For the first alkene, consider an alkene where the double bond is between the tertiary carbon (where the -OH group will be attached) and one of its neighboring carbons. Acid-catalyzed hydration will add the -OH group to the more substituted carbon (Markovnikov addition). Example: 1-methylcyclopentene.
Step 4: For the second alkene, consider an alkene where the double bond is between the tertiary carbon and a different neighboring carbon. Hydroboration-oxidation can be used to add the -OH group to the less substituted carbon (anti-Markovnikov addition). Example: 2-methylcyclopentene.
Step 5: Ensure that the reaction conditions are appropriate for each synthesis method. For acid-catalyzed hydration, use H₂SO₄ and water. For hydroboration-oxidation, use BH₃ followed by H₂O₂ and NaOH.

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