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The possible number of stereoisomers of ...

The possible number of stereoisomers of the product of following reaction would be :
`Ph-CH=CH-undersetunderset(CH_3)(|)CH-CHOoverset(NH_2OH)to`

A

2

B

4

C

6

D

8

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AI Generated Solution

The correct Answer is:
To determine the possible number of stereoisomers for the product of the given reaction, we will follow these steps: ### Step 1: Identify the Reaction The reaction involves the compound `Ph-CH=CH(CH₃)CH-CHO` being treated with hydroxylamine (NH₂OH). The product will be an oxime formed from the carbonyl group (CHO). ### Step 2: Analyze the Structure The starting compound has a double bond (alkene) and a carbonyl group. The presence of these functional groups suggests that we will have stereocenters in the product. ### Step 3: Identify Stereocenters 1. **Alkene (C=C)**: The double bond between the two carbon atoms allows for cis/trans (E/Z) isomerism. This gives us one stereocenter. 2. **Carbon attached to the carbonyl (C=O)**: The carbon atom bonded to the nitrogen from hydroxylamine will also serve as a stereocenter because it will have four different substituents after the reaction (Ph, CH₃, OH, and NH). 3. **The carbon adjacent to the double bond**: This carbon is also a stereocenter because it has different groups attached (Ph, CH₃, and the carbon chain). ### Step 4: Count the Stereocenters From the analysis: - We have identified **3 stereocenters** in the product. ### Step 5: Calculate the Number of Stereoisomers The formula to calculate the number of stereoisomers based on the number of stereocenters (n) is given by: \[ \text{Number of stereoisomers} = 2^n \] Where n is the number of stereocenters. In this case: \[ n = 3 \] So, \[ \text{Number of stereoisomers} = 2^3 = 8 \] ### Conclusion The possible number of stereoisomers of the product is **8**.

To determine the possible number of stereoisomers for the product of the given reaction, we will follow these steps: ### Step 1: Identify the Reaction The reaction involves the compound `Ph-CH=CH(CH₃)CH-CHO` being treated with hydroxylamine (NH₂OH). The product will be an oxime formed from the carbonyl group (CHO). ### Step 2: Analyze the Structure The starting compound has a double bond (alkene) and a carbonyl group. The presence of these functional groups suggests that we will have stereocenters in the product. ...
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