Provide the expected product for the reaction of each of the following alkenes with H₂SO₄ and H₂O.
(b)

Verified step by step guidance

1. Step 1: Identify the functional group in the given molecule. The structure contains an alkene functional group (a double bond) in a cyclic compound.
2. Step 2: Understand the reaction conditions. The reaction involves H2SO4 (sulfuric acid) and H2O (water), which typically leads to an acid-catalyzed hydration of the alkene. This reaction follows Markovnikov's rule.
3. Step 3: Apply Markovnikov's rule. In acid-catalyzed hydration, the hydrogen atom from H2O will add to the carbon of the double bond with more hydrogens (less substituted), and the hydroxyl group (-OH) will add to the carbon with fewer hydrogens (more substituted).
4. Step 4: Consider carbocation stability. During the reaction, a carbocation intermediate is formed. The stability of the carbocation is crucial, and rearrangements may occur to form a more stable carbocation (e.g., tertiary carbocation).
5. Step 5: Draw the expected product. After the addition of H2O, the double bond is replaced by a single bond, and an -OH group is added to the more substituted carbon of the original double bond, resulting in an alcohol product.

Key Concepts

Electrophilic Addition

Electrophilic addition is a fundamental reaction mechanism in organic chemistry where an electrophile reacts with a nucleophile, typically involving alkenes. In the presence of strong acids like H₂SO₄, the double bond of the alkene acts as a nucleophile, attacking the electrophilic hydrogen, leading to the formation of a carbocation intermediate. This step is crucial for understanding how alkenes react with acids and water.

Carbocation Stability

Carbocation stability is a key concept in organic reactions, as the stability of the carbocation intermediate significantly influences the reaction pathway and product formation. Carbocations can be classified as primary, secondary, or tertiary, with tertiary carbocations being the most stable due to hyperconjugation and inductive effects. Understanding the stability of these intermediates helps predict the major product of the reaction.

Hydration Reaction

The hydration reaction involves the addition of water (H₂O) to an alkene, resulting in the formation of an alcohol. In the context of the reaction with H₂SO₄, the acid first protonates the alkene to form a carbocation, which is then attacked by water. This process is essential for converting alkenes into alcohols and is a common method for synthesizing alcohols in organic chemistry.