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Statement-I : Solubility on n-alcohols i...

Statement-I : Solubility on n-alcohols in water decreases with increase in molecular weight
Because
Statement-II: The relative proportion of the hydrocarbon part in alcohols increases with increasing molecular weight which permits enhanced hydrogen bond with water.

A

Statement-I is True, Statement-II is True : Statement-II is a correct explanation for Statement-I

B

Statement-I is True, Statement-II is True : Statement-II is `NOT` a correct explanation for Statement-I

C

Statement-I is True, Statement-II is False.

D

Statement-I is False, Statement-II is True.

Text Solution

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The correct Answer is:
C
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Statement I Solubility of n-alcohol in water decreases with increase in molecular weight. Statement II The relative proportion of the hydrocarbon part in alcohols increases with increasing molecular weight which permit enhanced hydrogen with water.

Statement I: The solubility of n-alcohol in water decrease with an increase in molecular weight. Statement II: The reactive proportion of the hydrocarbon part in alcohols increase with increasing molecular weight which permits enthanced hydrogen bonding with water.

Solubility of alcohol in water increases with

The boiling points of halogens increase with increase in molecular weight, it is because

Statement -1 Solubility of alcohols decreases with increasing molecular weight Statement -2 : Increases in hydrophobic group decreases proportion of hydrogen bonding .

Assertion: Solubility of n -alcohol in water decreases with increases in molar mass. Reason: The hydrophobic neture of alky 1 chain increases.

ALLEN-ALKENE, ALKANE & ALKYNE -EXERCISE-3
  1. A third group is least likely to enter between two groups in the meta ...

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  2. A third group is least likely to enter between two groups in the meta ...

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  3. Statement-I : Solubility on n-alcohols in water decreases with increas...

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  4. Statement I: p-Nitrophenol is a stronger acid than o-nitrophenol. St...

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  5. Statement-I: Phenol is more reactive than benzene towards electrophili...

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  6. Statement-I: Tert-Butoxide is a stronger base than OH^(-) or C(2)H(5)O...

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  7. Statement-I With Br(2)//H(2)O phenol give 2,4,6- tribromophenol but wi...

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  8. Phenols are converted into their salts by aqueous NaOH but not by aque...

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  9. Phenols are converted into their salts by aqueous NaOH but not by aque...

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  10. Phenols are converted into their salts by aqueous NaOH but not by aque...

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  11. Phenols are converted into their salts by aqueous NaOH but not by aque...

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  12. Phenols are converted into their salts by aqueous NaOH but not by aque...

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  13. Symmetrically subsituted epoxides give the same products in both the a...

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  14. Symmetrically subsituted epoxides give the same products in both the a...

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  15. Symmetrically subsituted epoxides give the same products in both the a...

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  16. Symmetrically subsituted epoxides give the same products in both the a...

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  17. Symmetrically subsituted epoxides give the same products in both the a...

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  18. When pinacol is treated with dilute H(2)SO(4), a re-arangement reactio...

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  19. When pinacol is treated with dilute H(2)SO(4), a re-arangement reactio...

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  20. When pinacol is treated with dilute H(2)SO(4), a re-arangement reactio...

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