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A mixture of 1-chlorobutane and 2-chloro...

A mixture of 1-chlorobutane and 2-chlorobutane when treated with alcoholic KOH gives:

A

1-butene

B

2-butene

C

isobutylene

D

mixture of 1-butene + 2 butene

Text Solution

AI Generated Solution

The correct Answer is:
To solve the problem of what products are formed when a mixture of 1-chlorobutane and 2-chlorobutane is treated with alcoholic KOH, we can follow these steps: ### Step 1: Identify the Reactants We have two reactants: 1. **1-chlorobutane (C4H9Cl)**: This has the structure CH3-CH2-CH2-CH2-Cl. 2. **2-chlorobutane (C4H9Cl)**: This has the structure CH3-CH2-CH(Cl)-CH3. ### Step 2: Understand the Reaction Condition The reaction is carried out in the presence of alcoholic KOH. Alcoholic KOH is a strong base that promotes elimination reactions, specifically beta-elimination (dehydrohalogenation), where HX (in this case, HCl) is eliminated. ### Step 3: Analyze the Reaction of 1-chlorobutane For **1-chlorobutane**: - The chlorine atom is attached to the first carbon (alpha carbon). - The beta carbon is the second carbon. - When KOH acts on 1-chlorobutane, it will remove a hydrogen atom from the beta carbon (C2) and eliminate HCl. The reaction can be represented as: \[ \text{CH}_3\text{CH}_2\text{CH}_2\text{CH}_2\text{Cl} + \text{KOH} \rightarrow \text{CH}_3\text{CH}_2\text{CH}=\text{CH}_2 + \text{HCl} \] The product formed is **but-1-ene** (C4H8). ### Step 4: Analyze the Reaction of 2-chlorobutane For **2-chlorobutane**: - The chlorine atom is attached to the second carbon (alpha carbon). - There are two beta carbons (C1 and C3). - KOH can remove a hydrogen atom from either beta carbon leading to two possible products. 1. If hydrogen is removed from C1: \[ \text{CH}_3\text{CH}_2\text{CHCl}\text{CH}_3 + \text{KOH} \rightarrow \text{CH}_3\text{CH}=\text{CH}\text{CH}_3 + \text{HCl} \] This product is **but-2-ene** (C4H8). 2. If hydrogen is removed from C3: \[ \text{CH}_3\text{CH}_2\text{CHCl}\text{CH}_3 + \text{KOH} \rightarrow \text{CH}_3\text{CH}_2\text{CH}=\text{CH}_2 + \text{HCl} \] This product is also **but-2-ene** (C4H8). ### Step 5: Combine the Products From the reactions above, we see that: - From 1-chlorobutane, we get **but-1-ene**. - From 2-chlorobutane, we get **but-2-ene**. Thus, the final products when a mixture of 1-chlorobutane and 2-chlorobutane is treated with alcoholic KOH are **but-1-ene** and **but-2-ene**. ### Final Answer The mixture of 1-chlorobutane and 2-chlorobutane when treated with alcoholic KOH gives **but-1-ene and but-2-ene**. ---
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OP TANDON-UNSATURATED HYDROCARBONS-OBJECTIVE QUESTIONS
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  7. The hydrocarbon, which can react with sodium in liquid ammonia is

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  8. Oxidation of 1-butene with hot KMnO(4) solution produces:

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  10. A compound 'X' on ozonolysis followed by reduction gives an aldehyde, ...

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  11. the number of alkynes possible with molecular formula C(5)H(8) is :

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  12. Hydration of which one of the following yields a ketone

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  13. One molecule of alkene 'X' on ozonolysis gave one mole of acetone. The...

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  14. One mole of alkene on ozonolysis gives 2 moles of butanone. The alkene...

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  15. Identify the alkyne in the following sequence of reactions: Alkyne o...

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  18. Me(2)C=CHCH(2)-underset(Me)underset(|)C=CH-CH(3)overset(H^(+))to'P' ...

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  19. One per cent composition of an organic compound A is carbon=85.71% and...

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