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How many optically active isomers of 2,3...

How many optically active isomers of 2,3-Dichlorobutandioic acid are possible ?

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To determine how many optically active isomers of 2,3-Dichlorobutanedioic acid are possible, we can follow these steps: ### Step 1: Draw the Structure Start by drawing the structure of 2,3-Dichlorobutanedioic acid. The molecular formula indicates that we have a butane backbone with two carboxylic acid groups (–COOH) and two chlorine substituents on the second and third carbon atoms. ### Step 2: Identify Chiral Centers Identify the chiral centers in the molecule. A chiral center is a carbon atom that is attached to four different groups. In 2,3-Dichlorobutanedioic acid, the second and third carbon atoms are chiral centers because they each have different substituents (–COOH, –Cl, –H, and the rest of the carbon chain). ### Step 3: Assign the Configuration Using the Cahn-Ingold-Prelog (CIP) priority rules, assign the configurations (R or S) to each chiral center: - For the second carbon (C2), assign priorities: Cl > COOH > H > the rest of the carbon chain. Depending on the arrangement, this could be either R or S. - For the third carbon (C3), assign priorities similarly. ### Step 4: Determine Optical Activity Next, determine the optical activity of the isomers: - If a molecule has a plane of symmetry, it is optically inactive. - If it does not have a plane of symmetry, it is optically active. ### Step 5: Count the Isomers Count the total number of stereoisomers. For a compound with 'n' chiral centers, the maximum number of stereoisomers is given by the formula \(2^n\). In this case, with 2 chiral centers, the maximum number of stereoisomers is \(2^2 = 4\). ### Step 6: Identify the Optically Active Isomers Out of the total isomers, identify which ones are optically active. - You will find that some of the isomers will be enantiomers (mirror images) and will be optically active. - Check for any meso compounds that may be present, which would be optically inactive due to internal symmetry. ### Conclusion After analyzing the configurations and symmetry, you will find that there are 2 optically active isomers of 2,3-Dichlorobutanedioic acid. ### Final Answer **There are 2 optically active isomers of 2,3-Dichlorobutanedioic acid.** ---

To determine how many optically active isomers of 2,3-Dichlorobutanedioic acid are possible, we can follow these steps: ### Step 1: Draw the Structure Start by drawing the structure of 2,3-Dichlorobutanedioic acid. The molecular formula indicates that we have a butane backbone with two carboxylic acid groups (–COOH) and two chlorine substituents on the second and third carbon atoms. ### Step 2: Identify Chiral Centers Identify the chiral centers in the molecule. A chiral center is a carbon atom that is attached to four different groups. In 2,3-Dichlorobutanedioic acid, the second and third carbon atoms are chiral centers because they each have different substituents (–COOH, –Cl, –H, and the rest of the carbon chain). ...
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