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Consider the given reaction CH(3)-unde...

Consider the given reaction
`CH_(3)-underset(CH_(3))underset(|)overset(CH_(3))overset(|)C-CH_(2)-OH overset("conc." H_(2)SO_(4))underset(Delta)to "Alkene(major)"`
Identify alkene.

A

`CH_(3)-CH_(2)-CH=CH_(2)`

B

`CH_(3)-CH=CH-CH_(3)`

C

`(CH_(3))_(2)C=C(CH_(3))_(2)`

D

`CH_(3)-CH=underset(CH_(3))underset(|)C-CH_(3)`

Text Solution

AI Generated Solution

The correct Answer is:
To identify the alkene formed from the given reaction, we will follow these steps: ### Step 1: Identify the starting compound The starting compound is 2-methyl-2-butanol, represented as: \[ \text{CH}_3 - \text{C(OH)(CH}_3) - \text{C(CH}_3) - \text{CH}_2 - \text{OH} \] ### Step 2: Understand the role of concentrated H2SO4 Concentrated sulfuric acid (H2SO4) acts as a dehydrating agent, which means it will remove a water molecule (H2O) from the alcohol to form an alkene. ### Step 3: Remove the hydroxyl group (OH) The hydroxyl group (OH) will be protonated by the concentrated H2SO4, making it a better leaving group. As a result, water (H2O) will be eliminated, leading to the formation of a carbocation. ### Step 4: Formation of carbocation When the OH group is removed, a carbocation is formed. In this case, we can have a primary carbocation (1°) or a tertiary carbocation (3°). The structure can be represented as: \[ \text{CH}_3 - \text{C}^+ - \text{CH}_3 - \text{CH}_2 \] ### Step 5: Evaluate carbocation stability The primary carbocation is less stable than the tertiary carbocation. Therefore, a methyl shift will occur from the adjacent carbon to stabilize the carbocation. This results in the formation of a more stable tertiary carbocation. ### Step 6: Rearrangement to form the stable carbocation After the methyl shift, the structure will look like this: \[ \text{CH}_3 - \text{C}^+ - \text{CH}_3 - \text{CH}_2 \] ### Step 7: Elimination of a proton (H) Now, a proton (H) will be eliminated from the carbon adjacent to the carbocation, resulting in the formation of a double bond. ### Step 8: Write the final alkene product The final alkene product formed from this reaction is: \[ \text{CH}_3 - \text{C} = \text{CH} - \text{CH}_3 \] This structure corresponds to 2-methylpropene. ### Final Answer The major alkene formed from the reaction is **2-methylpropene**. ---
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AAKASH INSTITUTE ENGLISH-HYDROCARBONS-Exercise
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  2. Bond angle in chair form of cyclohexane is

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  3. Most stable conformation of n-butane is :

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  4. Torsion strain is the repulsive interaction between

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  5. Which form (s) of cyclohexane is/are free from angle strain?

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  6. The number of axial hydrogen atoms in chair form of cyclohexane is

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  7. Consider the given reaction CH(3)-underset(CH(3))underset(|)overset(...

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  8. Ethylene reacts with S(2)Cl(2) to give

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  9. Actylene reacts with ammonical Cu(2)Cl(2) to give precipitate of

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  10. Identify the product in the reaction HC-=CH overset(K(2)Cr(2)O(7)+H(...

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  11. Which of the following compound gives CO(2) on reductive ozonolysis-

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  12. The carbon-carbon bond length in benzene molecule is:

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  13. The product formed in the reaction, Product is

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  14. Which of the following is the most reactive towards nucleophilic subst...

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  15. Which of the following is aromatic in nature ?

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  16. Which of the following is used for the preparation of benzene ?

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  17. Which of the following is an examples of Friedel Crafts reaction ?

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  18. Which of the following is aromatic hydrocarbon ?

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  19. The following of pie and sigma bonds in touleneis repectively

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  20. The C-C-C bond angle in benzene is

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