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Arrangements of (CH(3))(3)C-,(CH(3))(2)C...

Arrangements of `(CH_(3))_(3)C-,(CH_(3))_(2)CH-,CH_(3).CH_(2)-` when attached to benzyl or `n` unsaturated group in increasing order of inductive effects is:

A

`(CH_(3))_(3)C^(-) lt (CH_(3))_(2)CH^(-) lt (CH_(3)).CH_(2)`

B

`CH_(3).CH_(2)^(-) lt (CH_(3))_(2)CH^(-) lt (CH_(3))_(3)C^(-)`

C

`(CH_(3))_(2)CH^(-) lt (CH_(3))_(3)C^(-) lt CH_(3).CH_(2)^(-)`

D

`(CH_(3))_(3)C^(-) lt CH_(3).CH_(2)^(-) lt (CH_(3))_(2)CH^(-)`

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To determine the increasing order of inductive effects for the groups `(CH₃)₃C-`, `(CH₃)₂CH-`, and `CH₃CH₂-` when attached to a benzyl or an unsaturated group, we can analyze the groups based on their ability to donate electron density through the inductive effect. ### Step-by-step Solution: 1. **Identify the Groups**: We have three groups to consider: - `(CH₃)₃C-` (tert-butyl group) - `(CH₃)₂CH-` (isopropyl group) - `CH₃CH₂-` (ethyl group) 2. **Understand Inductive Effect**: The inductive effect refers to the electron-donating or withdrawing effect of substituents through sigma bonds. Groups that can donate electrons will have a positive inductive effect (+I), while groups that withdraw electrons will have a negative inductive effect (-I). 3. **Evaluate Each Group**: - **(CH₃)₃C-**: This group has three methyl groups. The presence of multiple methyl groups increases the electron density through hyperconjugation and inductive effects, making it a strong electron-donating group. - **(CH₃)₂CH-**: This group has two methyl groups. It also donates electron density but to a lesser extent than the tert-butyl group. - **CH₃CH₂-**: This group has one methyl group and is the weakest in terms of inductive effect among the three groups. 4. **Rank the Groups**: Based on the number of methyl groups and their ability to donate electron density, we can rank the groups in increasing order of their inductive effects: - `CH₃CH₂-` (weakest inductive effect) - `(CH₃)₂CH-` (moderate inductive effect) - `(CH₃)₃C-` (strongest inductive effect) 5. **Final Arrangement**: Therefore, the increasing order of inductive effects when attached to benzyl or an unsaturated group is: - `CH₃CH₂- < (CH₃)₂CH- < (CH₃)₃C-`

To determine the increasing order of inductive effects for the groups `(CH₃)₃C-`, `(CH₃)₂CH-`, and `CH₃CH₂-` when attached to a benzyl or an unsaturated group, we can analyze the groups based on their ability to donate electron density through the inductive effect. ### Step-by-step Solution: 1. **Identify the Groups**: We have three groups to consider: - `(CH₃)₃C-` (tert-butyl group) - `(CH₃)₂CH-` (isopropyl group) - `CH₃CH₂-` (ethyl group) ...
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A2Z-SOME BASIC PRINCIPALS OF ORGANIC CHEMISTRY-Section D - Chapter End Test
  1. Arrangements of (CH(3))(3)C-,(CH(3))(2)CH-,CH(3).CH(2)- when attached ...

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  2. Arrange the following comounds in increasing order of length of their ...

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  3. The order of heat of hydrogenation in following compounds is:

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  4. S(N)1 reaction is faster in

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  5. Which compound would be least soluble in water?

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  6. Among the following compound which can be dehydrated very easily is :

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  7. Which of the follwing is not the characteristic of the mechanism of fr...

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  8. Find the strongest acid among the following compound

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  9. Among the following the dissociation constant is highest

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  10. Which one of the following compounds is most acidic

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  11. The optically active tartaric acid is named as D-(+)- tartaric acid be...

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  12. Among the following compounds (I-II) the correct order of reaction wit...

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  13. The following reaction is described as

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  14. Which of the following is the most stable cation?

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  15. The observed dipole moment of nitromethane is highly than the dipole m...

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  16. Dehydrohalogenation in presence of OH^(-) is correct represented by

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  17. Among the following the aromatic compound is

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  18. Which of the following compounds are not arranged in order of decreasi...

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  19. Most stable carbonium ion is :

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  20. Which one of the following species is most stable

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  21. Which of the following gives most stable carbocation by dehydration

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