Predict the products and propose mechanisms for the following reactions.
(a)

Guida verificata passo dopo passo

Step 1: Recognize the functional group in the reactant. The molecule contains an ester functional group, which is characterized by the -COOR structure. Esters are susceptible to hydrolysis under acidic conditions.

Step 2: Understand the reaction conditions. The presence of H⁺/H₂O indicates that the reaction will proceed via acid-catalyzed hydrolysis of the ester. This involves breaking the ester bond to form a carboxylic acid and an alcohol.

Step 3: Protonation of the ester oxygen. The reaction begins with the protonation of the carbonyl oxygen by H⁺, increasing the electrophilicity of the carbonyl carbon and making it more susceptible to nucleophilic attack.

Step 4: Nucleophilic attack by water. A water molecule acts as a nucleophile and attacks the carbonyl carbon, forming a tetrahedral intermediate. This intermediate will rearrange and lose the alcohol group (ethanol in this case).

Step 5: Formation of products. The final products of the reaction are a carboxylic acid (derived from the ester) and ethanol (derived from the alkoxy group of the ester).

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Ester Hydrolysis

Ester hydrolysis is a chemical reaction where an ester reacts with water in the presence of an acid or base to form an alcohol and a carboxylic acid. In acid-catalyzed hydrolysis, the acid protonates the carbonyl oxygen of the ester, increasing its electrophilicity and facilitating the nucleophilic attack by water. This reaction is crucial in organic chemistry for understanding the behavior of esters in various conditions.

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Acid Catalysis

Acid catalysis involves the use of an acid to increase the rate of a chemical reaction. In the context of ester hydrolysis, the acid donates a proton to the carbonyl oxygen, enhancing the electrophilic character of the carbonyl carbon. This makes it more susceptible to nucleophilic attack by water, thus accelerating the hydrolysis process. Understanding acid catalysis is essential for predicting reaction mechanisms and product formation.

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Reaction Mechanism

A reaction mechanism is a step-by-step description of the pathway through which reactants are converted into products. It includes the sequence of bond-breaking and bond-forming events, intermediates, and transition states. For ester hydrolysis, the mechanism typically involves protonation of the ester, nucleophilic attack by water, and subsequent deprotonation to yield the final products. Analyzing mechanisms helps in predicting the outcomes of chemical reactions.

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