JEE Main 20265 AprilMorning Shift
- Exam
- JEE Main
- Year
- 2026
- Date
- 5 April
- Shift
- Morning Shift
- Subject
- Chemistry
- Chapter
- Alcohols Phenols and Ethers
JEE Main 2026 · 5 April · Morning Shift · Chemistry · Alcohols Phenols and Ethers
Consider compounds A, B and C with following structural formulae A...
Consider compounds A, B and C with following structural formulae
CH - CH - CH - CH - CH - OH
CH CH - CH - CH - CH
HO - CH - CH - CH(OH) - CH
For the conversion of B from A, reagent (D) required is _________ and structural formula of product (E) obtained when C undergoes same reaction using excess reagent (D) is _________.
CH - CH - CH - CH - CH - OH
CH CH - CH - CH - CH
HO - CH - CH - CH(OH) - CH
For the conversion of B from A, reagent (D) required is _________ and structural formula of product (E) obtained when C undergoes same reaction using excess reagent (D) is _________.
Options
- A
D E Conc. HSO CH CH CH(OH)CH - B
D E PCC HO CH CH CH = CH - C
D E PCC CH CH CH = CH - D
D E Conc. HSO or HPO CH CH CH = CH
Correct answer
D.
| D | E |
| Conc. HSO or HPO | CH CH CH = CH |
Step-by-step solution
Compound A is pen\tan^{-1}-ol () and Compound B is pent-1-ene ().
The conversion of an alcohol to an alkene is a dehydration reaction, which requires an acidic dehydrating agent such as concentrated or . Thus, reagent D is concentrated or .
Compound C is butane-1,3-diol ().
When C is treated with excess dehydrating agent (reagent D), both hydroxyl groups undergo elimination (dehydration). The elimination of two water molecules yields a conjugated diene, which is highly stable due to resonance.
The product E formed is 1,3-butadiene ().
Answer:
The conversion of an alcohol to an alkene is a dehydration reaction, which requires an acidic dehydrating agent such as concentrated or . Thus, reagent D is concentrated or .
Compound C is butane-1,3-diol ().
When C is treated with excess dehydrating agent (reagent D), both hydroxyl groups undergo elimination (dehydration). The elimination of two water molecules yields a conjugated diene, which is highly stable due to resonance.
The product E formed is 1,3-butadiene ().
Answer:
| D | E |
| Conc. HSO or HPO | CH CH CH = CH |