Before You Begin
Question #44605
The Question
Consider the reaction of solid pentacarbonylchloromanganese(I), , with a solution of methylmagnesium bromide () in THF at 298 K to form an intermediate organometallic complex . Subsequent heating of with one equivalent of triphenylphosphine () in a non-polar solvent yields complex . Assuming all major complexes obey the 18-electron rule, identify the structures of and .
Options
- A.
,
- B.
,
- C.
,
- D.
,
Check Your Answer
Correct Answer
Step-by-Step Solution
Explanation
How the Examiner Thinks
Mechanism_Trap
Don't get tricked by the process! Learn the mechanical traps used in competitive exam questions.
Concepts Behind This Question
Synergic Bonding in Carbonyls|Grignard Reagent Sensitivity|Nucleophilic Acyl Substitution
Why This Question Is Tricky
Common Mistakes
The trap exploits the student's organic chemistry bias.
When presented with a Grignard reagent and a carbonyl-containing compound, students instinctively predict nucleophilic acyl substitution at the carbonyl carbon (Option B).
However, in transition metal carbonyls, synergic -backbonding increases electron density on the CO carbon, rendering it less electrophilic.
The metal center, bearing a leaving group (), is the actual electrophilic site.
Furthermore, students must recognize that ligand substitution in alkyl carbonyl complexes typically proceeds via migratory insertion rather than direct CO displacement (Option C).
Quick Facts About This Question
Question Information
| Subject | Chemistry |
| Chapter | Coordination Compounds - Class 12 |
| Concept | Synergic Bonding in Carbonyls |
| Difficulty | 8 |
| Cognitive Load | 7 |
| Target Solve Time | 160 sec |
| Access | Free |