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CH(3)COOH overset((i) PCl(3)+Cl(2) ("exc...

`CH_(3)COOH overset((i) PCl_(3)+Cl_(2) ("excess"))underset((ii) O_(2))to (X) overset(SOCl_2) to (Y) overset(H_(2)//Pd//BaSO_(4))to(Z) overset(OH^(-))to W+S `
Write the structure of X,Y,Z , W and S

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To solve the problem step by step, we will analyze each reaction and determine the structures of the compounds X, Y, Z, W, and S formed during the reactions of acetic acid (CH₃COOH). ### Step 1: Reaction of CH₃COOH with PCl₃ and Cl₂ (excess) to form X The first reaction involves acetic acid (CH₃COOH) reacting with phosphorus trichloride (PCl₃) and chlorine (Cl₂) in excess. This is known as the HVZ reaction (Hunsdiecker reaction). **Resulting Compound (X):** The product formed is chloroacetic acid (ClCH₂COOH). **Structure of X:** ``` Cl | H2C - C - OH || O ``` ### Step 2: Reaction of X with SOCl₂ to form Y Next, chloroacetic acid (X) reacts with thionyl chloride (SOCl₂). This reaction converts the carboxylic acid group into an acyl chloride. **Resulting Compound (Y):** The product formed is acetyl chloride (CH₃COCl). **Structure of Y:** ``` Cl | H3C - C || O ``` ### Step 3: Reaction of Y with H₂/Pd/BaSO₄ to form Z The acetyl chloride (Y) then undergoes reduction in the presence of hydrogen gas (H₂) and a palladium catalyst supported on barium sulfate (BaSO₄). This is a Rosenmund reduction. **Resulting Compound (Z):** The product formed is acetaldehyde (CH₃CHO). **Structure of Z:** ``` H | H3C - C || O ``` ### Step 4: Reaction of Z with OH⁻ to form W and S Finally, acetaldehyde (Z) reacts with hydroxide ions (OH⁻) in a reaction known as aldol condensation. This reaction typically leads to the formation of β-hydroxy aldehydes or ketones. **Resulting Compound (W):** The product formed is 3-hydroxybutanal (W), which has both an aldehyde and an alcohol functional group. **Structure of W:** ``` H | H2C - C - OH | || O O ``` **Resulting Compound (S):** The byproduct (S) of this reaction is hydrochloric acid (HCl). ### Summary of Structures: - **X:** Chloroacetic acid (ClCH₂COOH) - **Y:** Acetyl chloride (CH₃COCl) - **Z:** Acetaldehyde (CH₃CHO) - **W:** 3-Hydroxybutanal (C₄H₈O₂) - **S:** Hydrochloric acid (HCl)
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