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Which one undergoes S(N)2 substitution r...

Which one undergoes `S_(N)2` substitution reaction faster and why?

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Since `I^(-)` ion is a better leaving group than `Cl^(-)` ion, therefore, reacts faster than in `S_(N)2` substitution reactions.
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PRADEEP-HALOALKANES AND HALOARENES-ADDITIONAL QUESTIONS (VERY SHORT ANSWER QUESTIONS)
  1. A solution of aqueous of KO hydrolysis CH(3)CHClCH(2)CH(3) and CH(3)CH...

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  2. In the pair, (CH(3))(3)C Cl and CH(3)Cl, CH(3)Cl will react faster in ...

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  3. Which one undergoes S(N)2 substitution reaction faster and why?

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  4. Out of two bromoderivatives C(6)H(5)CH(CH(3))Br and C(6)H(5)CH(C(6)H...

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  5. Which compound in each of the following pairs will react faster by S(N...

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  6. What is the reagent used for dehydrohalogenation of an alkyl halide?

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  7. Write a chemical reaction to illustrate Saytzeff's rule.

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  8. How do you convert: 2-Bromobutane to but-2-ene?

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  9. Name the alkyl halide which can be used to prepare methane and ethane ...

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  10. What is meant by plane polarized light ? What type of waves show this ...

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  11. What is an asymmetric or chiral carbon?

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  12. What is the condition to be satisfied for a compound to be chiral?

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  13. What type of isomerism is shown by lactic acid.

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  14. What do prefixes (+),(-) and (+-) before an organic compound mean?

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  15. What is a racemic mixture? Give an example

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

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

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

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

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

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