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Question #44474
The Question
Acetylene () exhibits terminal acidity due to its sp-hybridized carbon atoms. It reacts with Tollens' reagent to form a highly insoluble silver acetylide () precipitate. To utilize as a controlled source of the nucleophile, excess solid is added to of pure water, and the system is allowed to reach equilibrium. Subsequently, of a solution is added to this suspension at . Given that the solubility product () of is at , calculate the new equilibrium concentration of the acetylide ion () in the final mixture. (Assume the volume is strictly additive and no hydrolysis of occurs).
Options
- A.
- B.
- C.
- D.
Check Your Answer
Correct Answer
Step-by-Step Solution
Explanation
How the Examiner Thinks
Exception_Exposure
Learn to identify edge cases and boundary exceptions that JEE examiners hide in math problems.
Concepts Behind This Question
Alkynes Terminal Acidity|Metal Activity Series Logic|Common Ion Effect on Solubility
Why This Question Is Tricky
Common Mistakes
The question tests the student's ability to integrate the concept of terminal alkyne acidity with the common ion effect in solubility equilibria.
The primary trap is the expression for silver acetylide (), which requires squaring the silver ion concentration ().
Students frequently forget to square the common ion concentration or fail to account for the dilution of the solution upon mixing (halving the concentration from to ).
Distractor B catches those who forget the dilution step, Distractor C catches those who forget the square term, and Distractor D catches those who calculate the pure water solubility, ignoring the common ion effect entirely.
Quick Facts About This Question
Question Information
| Subject | Chemistry |
| Chapter | Hydrocarbons - Class 11 Part 2 |
| Concept | Alkynes Terminal Acidity |
| Difficulty | 8 |
| Cognitive Load | 7 |
| Target Solve Time | 160 sec |
| Access | Free |