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Which pair is identical ?...

Which pair is identical ?

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To determine which pair of compounds is identical, we will analyze each pair systematically based on their structural configurations and stereochemistry. ### Step-by-Step Solution: 1. **Identify the First Pair:** - The first compound has two methyl groups attached to the same carbon. - Since there are no chiral centers in this molecule, it is symmetrical. - Thus, both structures are identical. 2. **Analyze the Second Pair:** - The second compound has a hydroxyl group (OH), a bromine (Br), and an ethyl group (Et) attached to two different carbon centers. - We need to determine the R/S configuration for both chiral centers. - For the first carbon: - Assign priorities: OH (1), Br (2), CH3 (3), H (4). - The configuration is clockwise (R) when H is in the back, but since H is in front, we flip it to S. - For the second carbon: - Assign priorities: Br (1), OH (2), Et (3), H (4). - The configuration is counterclockwise (S) when H is in the back, but since H is in front, we flip it to R. - Since the configurations are different (R and S), these compounds are not identical. 3. **Examine the Third Pair:** - The third compound has two hydroxyl groups and we need to analyze their configurations. - If we rotate one of the molecules by 180 degrees, we find that the positions of the OH groups swap. - This results in an enantiomer relationship, indicating that they are not identical. 4. **Evaluate the Fourth Pair:** - The fourth compound also has two chiral centers. - For the first carbon: - Assign priorities: Br (1), Cl (2), CH3 (3), H (4). - The configuration is counterclockwise (S). - For the second carbon: - Assign priorities: Br (1), Cl (2), CH3 (3), H (4). - The configuration is clockwise (R). - Since one is S and the other is R, these compounds are also not identical. ### Conclusion: The only pair that is identical is the **first pair** of compounds. The other pairs are either enantiomers or different molecules. ---

To determine which pair of compounds is identical, we will analyze each pair systematically based on their structural configurations and stereochemistry. ### Step-by-Step Solution: 1. **Identify the First Pair:** - The first compound has two methyl groups attached to the same carbon. - Since there are no chiral centers in this molecule, it is symmetrical. - Thus, both structures are identical. ...
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RESONANCE ENGLISH-STEREOISOMERISM-EXERCISE (ADDITIONAL PROBLEMS FOR SELF PRACTICE (APSP)) PART 1
  1. Which type of isomerism is shown by 2, 3-Dichlorobutane ?

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  2. Increasing order of stability among the three main conformation ( i.e....

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  3. The unusually stable three membered unsaturated compound, Feist acid w...

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  4. Which of the following depict the same ?

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  5. The total number of chiral centres present in the artificial sweetener...

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  6. Which pair is identical ?

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  7. Identify the relation between molecules given in Newman and Fischer pr...

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  8. The correct IUPAC name of D-Glucose is :

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  9. Which of the following species will be optically active ?

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  10. Which of the following compounds exhibits stereoisomerism?

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  11. The isomeric alcohol which has a chiral carbon atom is :1

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  12. Which of the following are intensive properties?

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  13. The R/S designation for the following stereoisomers of 1,3-dichloro-2-...

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  14. Which of the following will not show geometrical isomerism?

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  15. The racemic mixture in liquid/gaseous state will have

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  16. True statement(s) regarding the given molecule is/are

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  17. The most stable conformation of cyclohexane is

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  18. The two compounds (I) and (II) are related as :

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  19. How many stereoisomers of a drug for healing the wounds are possible &...

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  20. Which of the following compunds is capable of showing geometrical, op...

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