Identify A through O:

Verified step by step guidance

1. Step 1: Analyze the starting material. The given compound is an alkene with a double bond between the second and third carbon atoms in a chain. The structure also includes a methyl group attached to the second carbon.
2. Step 2: Recognize the reaction type. The reagents R₂BH/THF followed by HO⁻, H₂O₂, and H₂O indicate a hydroboration-oxidation reaction. This reaction converts an alkene into an alcohol.
3. Step 3: Understand the regioselectivity of hydroboration. Hydroboration-oxidation follows anti-Markovnikov addition, meaning the hydroxyl group (-OH) will attach to the less substituted carbon of the double bond.
4. Step 4: Predict the intermediate. In the first step, the boron reagent (R₂BH) adds to the less substituted carbon of the double bond, forming an organoborane intermediate.
5. Step 5: Describe the final product. In the second step, oxidation with H₂O₂ and HO⁻ replaces the boron atom with a hydroxyl group (-OH), resulting in the formation of an alcohol at the less substituted carbon of the original double bond.

Key Concepts

Hydroboration-Oxidation

Hydroboration-oxidation is a two-step reaction process used to convert alkenes into alcohols. The first step involves the addition of borane (BH3) to the alkene, forming an organoborane intermediate. In the second step, this intermediate is oxidized using hydrogen peroxide (H2O2) and hydroxide ions (OH-), resulting in the formation of an alcohol with anti-Markovnikov selectivity.

Anti-Markovnikov Addition

Anti-Markovnikov addition refers to the regioselectivity observed in certain reactions, where the less substituted carbon of an alkene receives the new substituent. In the context of hydroboration, this means that the boron atom attaches to the less substituted carbon, leading to the formation of an alcohol at that position after oxidation, which is contrary to the typical Markovnikov rule.

Reagents and Solvents

The choice of reagents and solvents is crucial in organic reactions. In hydroboration, R2BH (dialkylborane) is used as the boron source, and THF (tetrahydrofuran) serves as a solvent that stabilizes the reaction intermediates. The subsequent oxidation step employs HO-, H2O2, and H2O, which are essential for converting the organoborane into the corresponding alcohol, highlighting the importance of solvent and reagent compatibility in reaction mechanisms.