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A diene on reductive ozonolysis produces...

A diene on reductive ozonolysis produces two moles of ethanal and one mole of propan -1,3-dial How many geometrical isomer (s) is/are possible for the diene?

A

2

B

3

C

4

D

6

Text Solution

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The correct Answer is:
To determine the number of geometrical isomers possible for the diene that produces 2 moles of ethanal and 1 mole of propan-1,3-diol upon reductive ozonolysis, we can follow these steps: ### Step 1: Identify the products The products of the reductive ozonolysis are: - 2 moles of ethanal (acetaldehyde, CH₃CHO) - 1 mole of propan-1,3-diol (CH₂(OH)CH(OH)CH₃) ### Step 2: Construct the corresponding alkene From the products, we can deduce the structure of the corresponding alkene. The presence of ethanal indicates that there are two carbonyl groups (C=O) and the propan-1,3-diol indicates that there are two hydroxyl groups (-OH) on the first and third carbon atoms of a three-carbon chain. To find the corresponding diene, we can visualize the structure: - Ethanal contributes two carbon atoms. - Propan-1,3-diol contributes three carbon atoms. Thus, the diene has a total of 5 carbon atoms. ### Step 3: Draw the diene structure The diene can be represented as follows: - C=C-C=C (where the double bonds are between the first and second, and the third and fourth carbon atoms). ### Step 4: Determine the possible geometrical isomers To find the geometrical isomers, we need to check for the presence of double bonds in the diene structure that can exhibit cis/trans (E/Z) isomerism. 1. **Identify double bonds**: In our diene structure, we have two double bonds. 2. **Check for substituents**: Each double bond must have different substituents to allow for geometrical isomerism. ### Step 5: Count the geometrical isomers For each double bond: - If we have different groups attached to the double bond, we can have both cis and trans forms. Assuming the diene has the following structure: - H₂C=CH-CH=CH₂ (with substituents on the ends) 1. For the first double bond (C1=C2), we can have: - Cis (both substituents on the same side) - Trans (substituents on opposite sides) 2. For the second double bond (C3=C4), we can also have: - Cis - Trans ### Step 6: Total geometrical isomers - For each double bond, we have 2 forms (cis and trans). - Therefore, if both double bonds can exhibit geometrical isomerism independently, we can calculate the total as follows: - 2 (from first double bond) x 2 (from second double bond) = 4 geometrical isomers. ### Conclusion Thus, the total number of geometrical isomers possible for the diene is **4**.

To determine the number of geometrical isomers possible for the diene that produces 2 moles of ethanal and 1 mole of propan-1,3-diol upon reductive ozonolysis, we can follow these steps: ### Step 1: Identify the products The products of the reductive ozonolysis are: - 2 moles of ethanal (acetaldehyde, CH₃CHO) - 1 mole of propan-1,3-diol (CH₂(OH)CH(OH)CH₃) ### Step 2: Construct the corresponding alkene ...
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