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The decreasing fugacity order of the fol...

The decreasing fugacity order of the following compounds is:
i. `PhSO_(3)^(o-)`, ii. `C_(2)H_(5)SO_(3)^(o-)`, iii. `C_(2)H_(5)COO^(o-)`, iv. `overset(o-)(C)N`, v. `overset(o-)(O)H`

A

`(v) gt (iv) gt (iii) gt (ii) gt (i)`

B

`(i) gt (ii) gt (iii) gt (iv) gt (v)`

C

`(iv) gt (v) gt (iii) gt (ii) gt (i)`

D

`(i) gt (ii) gt (iii) gt (v) gt (iv)`

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The correct Answer is:
To determine the decreasing fugacity order of the given compounds, we can analyze their basic strength and subsequently their leaving group ability. Here’s a step-by-step solution: ### Step 1: Identify the Compounds The compounds given are: 1. `PhSO3^-` (Phenyl sulfonate) 2. `C2H5SO3^-` (Ethyl sulfonate) 3. `C2H5COO^-` (Ethanoate) 4. `CN^-` (Cyanide) 5. `OH^-` (Hydroxide) ### Step 2: Determine Conjugate Acids To analyze the basic strength, we first determine the conjugate acids of each compound by adding a proton (H⁺): 1. `PhSO3^-` → `PhSO3H` (Phenyl sulfonic acid) 2. `C2H5SO3^-` → `C2H5SO3H` (Ethyl sulfonic acid) 3. `C2H5COO^-` → `C2H5COOH` (Propanoic acid) 4. `CN^-` → `HCN` (Hydrogen cyanide) 5. `OH^-` → `H2O` (Water) ### Step 3: Analyze Acidic Strength Now we will analyze the acidic strength of these conjugate acids: - **Sulfonic acids** (like `PhSO3H` and `C2H5SO3H`) are generally stronger acids than **carboxylic acids** (like `C2H5COOH`). - Among sulfonic acids, `PhSO3H` is more acidic than `C2H5SO3H` due to the electron-withdrawing effect of the phenyl group. - `C2H5COOH` is less acidic than both sulfonic acids but more acidic than `HCN` and `H2O`. - `HCN` is less acidic than `C2H5COOH`, and `H2O` is the least acidic. Thus, the order of acidic strength is: 1. `PhSO3H` (most acidic) 2. `C2H5SO3H` 3. `C2H5COOH` 4. `HCN` 5. `H2O` (least acidic) ### Step 4: Determine Basic Strength The basic strength is inversely related to acidic strength. Therefore, the basic strength order is: 1. `OH^-` (most basic) 2. `CN^-` 3. `C2H5COO^-` 4. `C2H5SO3^-` 5. `PhSO3^-` (least basic) ### Step 5: Determine Leaving Group Strength The leaving group ability is also inversely related to basic strength. Thus, the order of leaving group strength (or fugacity order) is: 1. `PhSO3^-` (strongest leaving group) 2. `C2H5SO3^-` 3. `C2H5COO^-` 4. `CN^-` 5. `OH^-` (weakest leaving group) ### Conclusion The decreasing fugacity order of the given compounds is: `PhSO3^- > C2H5SO3^- > C2H5COO^- > CN^- > OH^-`

To determine the decreasing fugacity order of the given compounds, we can analyze their basic strength and subsequently their leaving group ability. Here’s a step-by-step solution: ### Step 1: Identify the Compounds The compounds given are: 1. `PhSO3^-` (Phenyl sulfonate) 2. `C2H5SO3^-` (Ethyl sulfonate) 3. `C2H5COO^-` (Ethanoate) 4. `CN^-` (Cyanide) ...
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The decreasing nucleophilic order of the following compounds is: i. PhSO_(3)^(o-) , ii. C_(2)H_(5)SO_(3)^(o-) , iii. C_(2)H_(5)COO^(o-) , iv. overset(o-)(C)N , v. overset(o-)(O)H

The decreasing basic order of the following is: i. PhSO_(3)^(o-) , ii. C_(2)H_(5)SO_(3)^(o-) , iii. C_(2)H_(5)COO^(o-) , iv. overset(o-)(C)N , v. overset(o-)(O)H

The decrasing fugacity order of the following compounds is: i. overset(o-)(C)H_(3) , ii. overset(o-)(O)H , iii. CH_(3)COO^(o-) , iv. H_(2)O

The decresing nuclephilic order of the following is: i. F_(3)CSO_(3)^(o-) , ii. Cl_(3)C-COO^(o-) iii. PhSO_(3)^(o-) , iv. MeSO_(3)^(o-)

The decreasing nucelophilic order of the following compounds is: i. overset(o-)(C)H_(3) , ii. overset(o-)(O)H , iii. CH_(3)COO^(o-) , iv. H_(2)O

The decreasing leaving group order of the following is: i. F_(3)CSO_(3)^(o-) , ii. Cl_(3)C-COO^(o-) iii. PhSO_(3)^(o-) , iv. MeSO_(3)^(o-)

The decarising basic order of the following is: i. F_(3)CSO_(3)^(o-) , ii. Cl_(3)C-COO^(o-) iii. PhSO_(3)^(o-) , iv. MeSO_(3)^(o-)

The decreasing basic order of the following is: i. overset(o-)(C)H_(3) , ii. overset(o-)(O)H , iii. CH_(3)COO^(o-) , iv. H_(2)O

The decreasing fugacity order of the following is: i. overset(o-)(C)N , ii. overset(o-)(O)H , iii. overset(o-)(O) Me , iv. overset(o-)(C)H_(3) , v. H^(o-)

The decreasing nucleophilic oder of the following compounds is: i. overset(o-)(C)H_(3) , ii. overset(o-)(N)H_(2) , iii. overset(o-)(O)H , iv. F^(o-)

CENGAGE CHEMISTRY ENGLISH-AROMATIC COMPOUNDS AND ALKYL AND ARYL HALIDES -Exercises Single Correct
  1. The decreasing basic order of the following is: i. PhSO(3)^(o-), ii....

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  2. The decreasing nucleophilic order of the following compounds is: i. ...

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  3. The decreasing fugacity order of the following compounds is: i. PhSO...

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  4. The decreaing basic order of the following is: i. overset(o-)(C)N, i...

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  5. The decreasing nucelophilc order of the following compounds is: i. o...

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  6. The decreasing fugacity order of the following is: i. overset(o-)(C)...

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  7. The decrasing basic order of the following is: i. Me(2)N - NMe(2), i...

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  8. Decreasing nucelophilic order of the following is: i. Me(2)N - Nme(2...

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  9. The decresing fugacity order of the following is: i. Me(2)N - Nme(2)...

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  10. underset("Specific rotation" = +50^(@))(Ph-CH(OH)CH(3)) overset(SOCl(2...

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  11. underset("Specific rotation" = +50^(@))(Ph-CH(OH)CH(3)) overset(SOCl(2...

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  12. underset("Specific rotation" = +50^(@))(Ph-CH(OH)CH(3)) overset(SOCl(2...

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  13. underset("Specific rotation" = +50^(@))(Ph-CH(OH)CH(3)) overset(SOCl(2...

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  14. CH(3) - CH(Cl) - C(2)H(5) overset(Alc.KOH)(rarr) CH(3) - CH = CH - CH(...

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  15. Alkyl halides can be obtained by all methods except

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  16. Neopentyl chloride on reaction with ethanolic KOH is likely to give

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  17. In the reaction CH(3)C equiv C^(-)Na^(+) + (CH(3))(2) CHCl rarr Prod...

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  18. In order to get ethanethiol from bromoethane, the reagent used is :

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  19. For the preparation of chloroethane,

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  20. X on treatment with sodium hydroxide followed by the addition of silve...

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