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Methylethylamine cannot be resolved into enantiomers because
(a)It is planar
(b)It undergoes rapid inversion
(c)It has a plane of symmetry
(d)A tricovalent atom cannot be a centre of chirality.

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Important Questions on Fundamentals of Organic Chemistry
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The Fischer projection of -erythrose is shown below.
-Erythrose and its isomers are listed as and in Column I. Choose the correct relationship of and with -erythrose from Column II.
Column - I | Column -II | ||
P. | ![]() |
1. | Diastereomer |
Q. | ![]() |
2. | Identical |
R. | ![]() |
3. | Enantiomer |
S. | ![]() |

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the compounds which can exhibit optical activity are :

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Which of the following alkenes can generate optically active compounds upon hydrogenation?

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