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The decreasing basic order of the follow...

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`

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)`

Text Solution

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The correct Answer is:
To determine the decreasing basic order of the given species, we will analyze the conjugate acids of each species and their relative acidity. The stronger the conjugate acid, the weaker the corresponding base will be. Here’s a step-by-step solution: ### Step 1: Identify the given species The species provided are: 1. \( \text{PhSO}_3^{-} \) (Phenyl sulfonate) 2. \( \text{C}_2\text{H}_5\text{SO}_3^{-} \) (Ethyl sulfonate) 3. \( \text{C}_2\text{H}_5\text{COO}^{-} \) (Ethanoate) 4. \( \text{CN}^{-} \) (Cyanide) 5. \( \text{OH}^{-} \) (Hydroxide) ### Step 2: Write the conjugate acids To find the basicity order, we need to write the conjugate acids of each species by adding a proton (\( H^{+} \)): 1. \( \text{PhSO}_3^{-} + H^{+} \rightarrow \text{PhSO}_3H \) (Benzene sulfonic acid) 2. \( \text{C}_2\text{H}_5\text{SO}_3^{-} + H^{+} \rightarrow \text{C}_2\text{H}_5\text{SO}_3H \) (Ethyl sulfonic acid) 3. \( \text{C}_2\text{H}_5\text{COO}^{-} + H^{+} \rightarrow \text{C}_2\text{H}_5\text{COOH} \) (Propanoic acid) 4. \( \text{CN}^{-} + H^{+} \rightarrow \text{HCN} \) (Hydrogen cyanide) 5. \( \text{OH}^{-} + H^{+} \rightarrow \text{H}_2\text{O} \) (Water) ### Step 3: Analyze the acidity of the conjugate acids Now, we will analyze the acidity of these conjugate acids: - **Benzene sulfonic acid** is more acidic than **ethyl sulfonic acid** due to the electron-withdrawing effect of the phenyl group. - **Ethyl sulfonic acid** is less acidic than both sulfonic acids but more acidic than **propanoic acid**. - **Propanoic acid** is more acidic than **hydrogen cyanide**. - **Hydrogen cyanide** is more acidic than **water**. ### Step 4: Determine the basicity order Since stronger acids correspond to weaker bases, we can now deduce the basicity order from the acidity of the conjugate acids: 1. \( \text{OH}^{-} \) (most basic, conjugate acid is water) 2. \( \text{CN}^{-} \) (second most basic, conjugate acid is HCN) 3. \( \text{C}_2\text{H}_5\text{COO}^{-} \) (third, conjugate acid is propanoic acid) 4. \( \text{C}_2\text{H}_5\text{SO}_3^{-} \) (fourth, conjugate acid is ethyl sulfonic acid) 5. \( \text{PhSO}_3^{-} \) (least basic, conjugate acid is benzene sulfonic acid) ### Final Order of Basicity Thus, the decreasing basic order is: \[ \text{OH}^{-} > \text{CN}^{-} > \text{C}_2\text{H}_5\text{COO}^{-} > \text{C}_2\text{H}_5\text{SO}_3^{-} > \text{PhSO}_3^{-} \]

To determine the decreasing basic order of the given species, we will analyze the conjugate acids of each species and their relative acidity. The stronger the conjugate acid, the weaker the corresponding base will be. Here’s a step-by-step solution: ### Step 1: Identify the given species The species provided are: 1. \( \text{PhSO}_3^{-} \) (Phenyl sulfonate) 2. \( \text{C}_2\text{H}_5\text{SO}_3^{-} \) (Ethyl sulfonate) 3. \( \text{C}_2\text{H}_5\text{COO}^{-} \) (Ethanoate) 4. \( \text{CN}^{-} \) (Cyanide) ...
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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

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 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 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 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 decreaing basic 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 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 basic order of the following is: i. overset(o-)(C)H_(3) , ii. overset(o-)(N)H_(2) , iii. overset(o-)(O)H , iv. F^(o-)

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

CENGAGE CHEMISTRY ENGLISH-AROMATIC COMPOUNDS AND ALKYL AND ARYL HALIDES -Exercises Single Correct
  1. The decreasing nucelophilic order of the following compounds is: i....

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  2. The decrasing fugacity order of the following compounds is: i. over...

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  3. The decreasing basic order of the following is: i. PhSO(3)^(o-), ii....

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

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

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

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

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

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

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

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  11. The decresing fugacity order of the following is: i. Me(2)N - Nme(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. underset("Specific rotation" = +50^(@))(Ph-CH(OH)CH(3)) overset(SOCl(2...

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

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

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  17. Alkyl halides can be obtained by all methods except

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

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

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

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