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Correct decreasing stability order of fo...

Correct decreasing stability order of following carbanions :
`""^(Ө)underset(" "I)(CH_(2))-CHO" "CH_(3)-underset(O)underset(||)C-""^(Ө)CH-underset(II" ")underset(O)underset(||)C-CH_(3)" "H-underset(III)underset(O)underset(||)-overset(Ө)(CH)-underset(O)underset(||)C-H" "OHC-underset(IV)underset(CHO)underset(|)overset(Ө)C-CHO`

A

`III gt IV gt II gt I`

B

`IV gt II gt III gt I`

C

`IV gt III gt II gt I`

D

`III gt II gt I gt IV`

Text Solution

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The correct Answer is:
To determine the correct decreasing stability order of the given carbanions, we will analyze each carbanion based on its structure and the effects of substituents on stability. ### Step-by-Step Solution: 1. **Identify the Type of Carbanion**: - **Carbanion I**: `CH2-CHO` - This carbanion has one carbon bonded to two hydrogens and one carbon. Thus, it is a **primary carbanion**. - **Carbanion II**: `CH3-C(=O)-CH` - This carbanion has one carbon bonded to one hydrogen and two carbons. Thus, it is a **secondary carbanion**. - **Carbanion III**: `H-C(=O)-C-CHO` - This carbanion has one carbon bonded to one hydrogen and two carbons. Thus, it is also a **secondary carbanion**. - **Carbanion IV**: `OHC-C(=O)-CHO` - This carbanion has one carbon bonded to three carbons. Thus, it is a **tertiary carbanion**. 2. **Determine Stability Based on Structure**: - The general order of stability for carbanions is: - Tertiary > Secondary > Primary - However, we must also consider the effects of substituents (electron-donating vs. electron-withdrawing). 3. **Analyze the Effects of Substituents**: - **Carbanion I** (Primary): Has one electron-withdrawing group (CHO), making it the least stable. - **Carbanion II** (Secondary): Has one electron-donating group (CH3) and one electron-withdrawing group (C=O). The presence of CH3 makes it more stable than Carbanion I. - **Carbanion III** (Secondary): Similar to Carbanion II but has two carbonyl groups (C=O), which are electron-withdrawing. This makes it less stable than Carbanion II. - **Carbanion IV** (Tertiary): Has three electron-withdrawing groups (CHO), making it the most stable due to the stabilization provided by the electron-withdrawing nature of the groups. 4. **Rank the Carbanions**: - Based on the analysis: - Carbanion IV (most stable) - Carbanion II (more stable than III) - Carbanion III (less stable than II) - Carbanion I (least stable) 5. **Final Order**: - The correct decreasing order of stability is: - **Carbanion IV > Carbanion II > Carbanion III > Carbanion I** - Thus, the order is **4 > 2 > 3 > 1**. ### Final Answer: The correct decreasing stability order of the carbanions is **4, 2, 3, 1**.
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RESONANCE ENGLISH-GENERAL ORGANIC CHEMISTRY II-Part-I : Only One Option Correct Type
  1. Arrange following compounds in decreasing order of their dipole moment...

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  2. Correct decreasing stability order of following carbanions : ""^(Ө)u...

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  3. Select the most stable intermediates :

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  4. Which of the following is most stable carbocation?

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  5. The most stable carbocation is:

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  6. The following carbocation rearranges to CH(2)=underset(CH(3))underse...

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  7. Correct basic strength order is :

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  8. The order of basic strength of the given basic nitrogen atoms is :

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  9. In the labelled N-atoms which is correct basic strength order:

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  10. Choose the strongest base among the following:

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  11. Select the basic strength order of following molecules ?

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  12. Which is the weakest base among the followings ?

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  13. Write the order of K(a(1)) values of following acids :

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  14. The acid strength order is :

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  15. (X) (C(6)H(3)CIBrCOOH) are a dihalosubstituted benzoic acids. The stro...

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  16. The order of acidity of the H-atoms underlined in the following compou...

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  17. Most acidic hydrogen is present in

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  18. The correct orders are:

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  19. Observe the following sequence of reactions : Select the correct ...

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  20. Order of K(a) which can be predicted by following reaction is:

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