Inductive Effect
Which order correctly represents decreasing +I (electron donating) inductive effect?
Select the correct option:
🔒 Solution Hidden from View
Submit your answer to unlock the detailed step-by-step solution.
More basic organic principles Practice Questions
Replacing a hydrogen of acetic acid with a strongly electron-withdrawing chlorine atom changes its a...
Replacing a hydrogen of acetic acid with a strongly electron-withdrawing chlorine atom changes its a...
Which of the following α-halo carboxylic acids is the strongest acid due to the inductive effect of ...
Which of the following α-halo carboxylic acids is the strongest acid due to the inductive effect of ...
The -I (negative inductive) effect is shown by:
The -I (negative inductive) effect is shown by:
In p-nitrophenol, nitro group reduces phenolic acidity via resonance or inductive effect?
In p-nitrophenol, nitro group reduces phenolic acidity via resonance or inductive effect?
Correct order of carbocation stability:
Correct order of carbocation stability:
Hybridization of carbon in benzene is:
Hybridization of carbon in benzene is:
Which is the correct acidity order (strongest acid first)?
Which is the correct acidity order (strongest acid first)?
Correct decreasing basicity order in aqueous solution:
Correct decreasing basicity order in aqueous solution:
In nitration of toluene, major products are:
In nitration of toluene, major products are:
Hyperconjugation is best described as:
Hyperconjugation is best described as:
Resonance stabilization is highest in:
Resonance stabilization is highest in:
Keto-enol tautomerism involves migration of:
Keto-enol tautomerism involves migration of:
About This Question
- Subject
- chemistry
- Chapter
- basic organic principles
- Topic
- inductive effect
- Difficulty
- Easy
- Year
- 2025
Solution
Correct Answer:
(CH3)3C− > (CH3)2CH− > CH3CH2− > CH3−
- Inductive Effect (I): The relative ability of an atom or group to either withdraw or donate electron density through σ bonds.
- Alkyl Groups: Higher alkyl groups act as electron-donating groups (+I effect).
- Reasoning: As the number of methyl groups attached to a central carbon increases, the collective electron-pushing ability increases due to both the inductive effect and hyperconjugation.
- Order:
- Tertiary (3∘): (CH3)3C− (Three methyl groups)
- Secondary (2∘): (CH3)2CH−
- Primary (1∘): CH3CH2−
- Methyl: CH3−
- Conclusion: The correct decreasing order is Tertiary > Secondary > Primary > Methyl.
This easy difficulty chemistry question is from the chapter basic organic principles, covering the topic of inductive effect. It appeared in the 2025 exam.
Looking for more practice? Explore all chemistry questions or browse basic organic principles questions on RankGuru.