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Optical activity is expected for ....

Optical activity is expected for .

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To determine which compound exhibits optical activity, we need to analyze the structures of the given acids: 2-methylpropenoic acid and 2-chloropropenoic acid. Optical activity arises from the presence of chiral centers in a molecule. A chiral center is typically a carbon atom that is sp3 hybridized and bonded to four different substituents. ### Step-by-Step Solution: 1. **Identify the Structures**: - **2-Methylpropenoic Acid**: The structure can be drawn as follows: - It has a double bond between the first and second carbon atoms, with a methyl group attached to the second carbon. - **2-Chloropropenoic Acid**: The structure can be drawn as follows: - It has a double bond between the first and second carbon atoms, with a chlorine atom and a methyl group attached to the second carbon. 2. **Determine Hybridization**: - For **2-methylpropenoic acid**, the second carbon (the one with the methyl group) is sp2 hybridized because it is involved in a double bond. - For **2-chloropropenoic acid**, the second carbon is also sp2 hybridized due to the presence of a double bond. 3. **Check for Chiral Centers**: - A chiral center must be sp3 hybridized and bonded to four different groups. - In **2-methylpropenoic acid**, the second carbon has two identical methyl groups, which means it does not have four different substituents. Therefore, it is not chiral. - In **2-chloropropenoic acid**, the second carbon is bonded to a chlorine atom, a methyl group, a hydrogen atom, and the rest of the molecule, making it a chiral center since all four substituents are different. 4. **Conclusion**: - Since only **2-chloropropenoic acid** has a chiral center, it is the only compound that exhibits optical activity. ### Final Answer: Optical activity is expected for **2-chloropropenoic acid**. ---
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