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Isopentane on monochlorination gives.......

Isopentane on monochlorination gives....isomers and out of them ....... Are optically active.

A

`3,1`

B

`4,2`

C

`3,2`

D

`4,1`

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The correct Answer is:
To solve the question regarding the monochlorination of isopentane, we will follow these steps: ### Step 1: Understand the Structure of Isopentane Isopentane, also known as 2-methylbutane, has the following structure: ``` CH3 | CH3-CH-CH2-CH3 | CH3 ``` This structure indicates that isopentane has a branched chain. ### Step 2: Identify Possible Monochlorination Products Monochlorination involves replacing one hydrogen atom with a chlorine atom. We can identify the positions where chlorine can be substituted: 1. Chlorination at the terminal carbon (C1). 2. Chlorination at the second carbon (C2). 3. Chlorination at the third carbon (C3). 4. Chlorination at one of the methyl groups (C4 or C5). ### Step 3: Draw the Monochlorination Products 1. **Chlorination at C1**: - Product: 1-chloro-2-methylbutane - Structure: ``` CH3 | CH3-CH-CH2-CH2Cl | CH3 ``` 2. **Chlorination at C2**: - Product: 2-chloro-2-methylbutane - Structure: ``` CH3 | CH3-C(Cl)-CH2-CH3 | CH3 ``` - This carbon is chiral, making this product optically active. 3. **Chlorination at C3**: - Product: 3-chloro-2-methylbutane - Structure: ``` CH3 | CH3-CH-CH(Cl)-CH3 | CH3 ``` - This carbon is not chiral, making this product optically inactive. 4. **Chlorination at a Methyl Group**: - Product: 2-chloro-3-methylbutane - Structure: ``` CH3 | CH2Cl-CH-CH3 | CH3 ``` - This carbon is chiral, making this product optically active. ### Step 4: Count the Isomers From the above analysis, we have identified a total of **4 monochlorination products**: 1. 1-chloro-2-methylbutane 2. 2-chloro-2-methylbutane (optically active) 3. 3-chloro-2-methylbutane (optically inactive) 4. 2-chloro-3-methylbutane (optically active) ### Step 5: Identify Optically Active Isomers Out of the four products, the following are optically active: 1. 2-chloro-2-methylbutane 2. 2-chloro-3-methylbutane Thus, we have **2 optically active isomers**. ### Final Answer Isopentane on monochlorination gives **4 isomers** and out of them **2 are optically active**.

To solve the question regarding the monochlorination of isopentane, we will follow these steps: ### Step 1: Understand the Structure of Isopentane Isopentane, also known as 2-methylbutane, has the following structure: ``` CH3 | CH3-CH-CH2-CH3 ...
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CENGAGE CHEMISTRY ENGLISH-AROMATIC COMPOUNDS AND ALKYL AND ARYL HALIDES -Exercises Single Correct
  1. Which of the following substrates will gave racemised product?

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  2. The energy of activation is lowest for which reaction?

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  3. Isopentane on monochlorination gives....isomers and out of them .........

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  4. Propane on dichlorinatin gives......isomers and out of them .....are o...

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  5. A solution of (+)2-chloro-2-phenylethane in toluene racemises slowly i...

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  6. The number of isomers for the compounds with molecular formula C(2)B...

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  7. The decreasing basic order of the following compounds is: i. NH(3)...

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  8. The decreasing nucleophilic order of the following compounds is: i...

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  9. The decreasing nucleophilic order of the following compounds is: i...

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  10. The decreasing basic order of the following is: i. F^(o-), ii. Cl^(o...

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  11. The decreasing nucleophillic order fo the following compounds is: i...

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  12. The decreasing leaving group order of the following is: i. F^(o-), i...

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  13. The decreasing basic order of the following is: i. overset(o-)(C)H(...

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  14. The decreasing nucleophilic oder of the following compounds is: i. o...

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  15. The deecreasing leaving group order of the following compounds is: ...

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  16. The decarising basic order of the following is: i. F(3)CSO(3)^(o-), ...

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  17. The decresing nuclephilic order of the following is: i. F(3)CSO(3)^(...

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  18. The decreasing leaving group order of the following is: i. F(3)CSO(3...

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  19. The decreasing basic order of the following compounds is: i. H(2)O, ...

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  20. The decasing nucleophilic order of the following compounds is: i. H(...

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