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When -CH(3), CH(3) - underset(CH(3))unde...

When `-CH_(3), CH_(3) - underset(CH_(3))underset(|)(CH) - " and " CH_(3) - underset(CH_(3))underset(|) overset(CH_(3))overset(|)C - ` groups are introduced on benzene ring then correct order of their inductive effect is

A

`CH_(3) - gt CH_(3) - underset(CH_(3))underset(|) (CH) - gt CH_(3) - underset(CH_(3))underset(|) overset(CH_(3))overset(|)C - `

B

` CH_(3) - underset(CH_(3))underset(|) overset(CH_(3))overset(|)C - gtCH_(3) - underset(CH_(3))underset(|)(CH) - gt CH_(3) - `

C

`CH_(3) - underset(CH_(3))underset(|) (CH) - gt CH_(3) gt CH_(3) - underset(CH_(3))underset(|) overset(CH_(3))overset(|)C - `

D

` CH_(3) - underset(CH_(3))underset(|) overset(CH_(3))overset(|)C - gt CH_(3) - gt CH_(3) - underset(CH_(3))underset(|) (CH) - `

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The correct Answer is:
To determine the correct order of the inductive effect of the given groups when introduced on a benzene ring, we need to analyze the groups one by one. The groups in question are: 1. **-CH3** 2. **-CH(CH3)2** (which can be interpreted as a carbon with one hydrogen and two methyl groups) 3. **-C(CH3)3** (a carbon with three methyl groups) ### Step-by-Step Solution: **Step 1: Analyze the first group (-CH3)** The -CH3 group (methyl group) has a weak +I (positive inductive) effect. This means it slightly pushes electron density towards the benzene ring but is not very strong in doing so. **Step 2: Analyze the second group (-CH(CH3)2)** The -CH(CH3)2 group has two methyl groups attached to a carbon, which increases the +I effect compared to a single -CH3 group. The two methyl groups will push more electron density towards the benzene ring than a single methyl group. **Step 3: Analyze the third group (-C(CH3)3)** The -C(CH3)3 group has three methyl groups attached to a single carbon. This group will exert the strongest +I effect among the three groups because it has the maximum number of methyl groups donating electron density towards the benzene ring. **Step 4: Compare the inductive effects** Now we can compare the inductive effects: - The -CH3 group has the weakest +I effect. - The -CH(CH3)2 group has a moderate +I effect. - The -C(CH3)3 group has the strongest +I effect. **Step 5: Establish the order of inductive effect** Based on the analysis: - The order of the inductive effect from weakest to strongest is: - **-CH3 < -CH(CH3)2 < -C(CH3)3** ### Final Answer: The correct order of their inductive effect is: **-CH3 < -CH(CH3)2 < -C(CH3)3** ---
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MOTION-GOC-Exercise - 1
  1. In which of the following molecules resonance takes place through out ...

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  2. The inductive effect

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  3. When -CH(3), CH(3) - underset(CH(3))underset(|)(CH) - " and " CH(3) - ...

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  4. Express in decreasing order of (+ I) - (a) CH(3)CH(2) - CH(2) - " ...

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  5. Consider the following carbanions (i) CH(3)- overset(Ө)CH(2)" "(ii...

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  6. In which of the following compounds is hydroxylic proton the most acid...

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  7. Consider following acid underset(I)(ClCH(2)COOH)," "underset(II)(C...

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  8. Which of the following acids has lowest pK(a) value?

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  9. Arrange in decreasing pK(a) (a) F - CH(2) CH(2) COOH (b)Cl - under...

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  10. The correct order of increasing acid strength of the compounds (a) C...

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  11. Correct order of basic strength in gas phase is (I) CH(3)-NH(2) (II...

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  12. Arrange basicity of the given compounds in decreasing order - (a)CH(...

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  13. Which one of the following is the strongest base in aqueous solution?

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  14. In which of the following molecules, all atoms are not coplanar ?

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  15. (I) CH(2) = CH - CH = CH(2) (II) overset(Theta)CH(2) - CH = CH - ove...

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  16. Among these canonical structures, the correct order of stability is

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  17. Amongt these canonical structures which one is least stable ?

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  18. For phenol which ofthe following resonating structure is the most stab...

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  19. The most stable resonating structure of following compound is

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  20. Among these canonical structures of pyridiine, the correct order of st...

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