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S(N)1 reactions are accompanied by racem...

`S_(N)1` reactions are accompanied by racemization in optically active halides.

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In `S_(N)1` reactions, carbocations are the intermediates. Since carbocations are planar species, therefore, attack of the nucleophile on them cann occur from both the sides (front and rear) with almost equal ease giving a 50:50 mixture of the two enantiomers, i.e., a racemix mixture is obtained.
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PRADEEP-HALOALKANES AND HALOARENES-ADDITIONAL QUESTIONS (VERY SHORT ANSWER QUESTIONS)
  1. What do prefixes (+),(-) and (+-) before an organic compound mean?

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  2. What is a racemic mixture? Give an example

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  3. S(N)1 reactions are accompanied by racemization in optically active ha...

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  4. What is the lowest molecular mass alkane that is chiral? Is there anot...

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  5. An acid of molecular formula, C(5)H(10)O(2) is optically active. What ...

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  6. A carboxylic acid of the formula, C(3)H(5)O(2)Br is optically active. ...

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  7. Give the structure of lowest molecular mass alcohol which is chiral?

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  8. C(C(6)H(12)), and optically active dydrocarbon which on catalytic hydr...

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  9. Which out of the two : 2-cyclopentenol or 3-cyclopentenol has chiral c...

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  10. Why is the seperation of lanthanoids difficult ?

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  11. Write a chemical reaction in which the iodide ion replaces the diazoni...

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  12. What effect should the following resonance of vinyl chloride have on i...

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  13. Why is vinyl chloride less reactive than ethyl chloride ?

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  14. Which of the following is most reactive toward nucleophilic substituti...

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  15. Give reasons: (i). C-Cl bond length in chlorobenzene is shorter than...

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  16. The dipole moment of vinyl chloride is lower than that of methyl chlor...

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  17. Grignard reagent of C(6)H(5)Cl can be prepared in THF but not in ether...

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  18. Give reasons: (a) n-Butyl bromide has higher boiling point than t-bu...

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  19. Arrange the following in the increasing order of ease of nucleo...

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  20. Give one example (with equation) wurtz-fittig reaction.

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