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Methylethylamine cannot be resolved into enantiomers because

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Important Questions on Fundamentals of Organic Chemistry

EASY
Which of the following acids does not exhibit optical isomerism?
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Which of the following compounds produces an optically inactive compound on hydrogenation? 
HARD

The Fischer projection of D-erythrose is shown below.

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D-Erythrose and its isomers are listed as P,Q,R, and S in Column I. Choose the correct relationship of P,Q,R, and S with D-erythrose from Column II.

  Column - I   Column -II
P. Question Image 1. Diastereomer
Q. Question Image 2. Identical
R. Question Image 3. Enantiomer
S. Question Image    

 

 

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Which of the following biphenyls is optically active?
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(+) 2-Methylbutan-1-ol and (-) 2- Methylbutan-1-ol have different values for which property?
EASY
The number of chiral centres present in threonine is _________
EASY
How many asymmetric carbon atoms are present in neopentyl chloride?
EASY
Which of the following molecules can exhibit optical activity?
EASY
An optically inactive racemic form can be separated into two active forms. This process is called
MEDIUM
Among i Cren33+, ii trans-Cren2Cl2+, iii Cis-Cren2Cl2+, iv CoNH34Cl2+ the optically active complexes are
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Which one of the following compounds is optically active?
EASY
Among the following.
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the compounds which can exhibit optical activity are :
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Identify the optically active cyclohexane from the given options.
EASY
The number of optically active isomers of the compound CH3CHBr-CHBr-COOH is
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Which of the following alkenes can generate optically active compounds upon hydrogenation?

Question Image

MEDIUM
The optically inactive compound from the following is: