Hofmann Elimination
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Q. 2-Bromopentane is heated with potassium ethoxide in ethanol. The major product obtained is
- 2-Ethoxypentane
- Pent-1-ene
- Cis-pent-2-ene
- Trans-pent-2-ene
Q.
The alkene formed as a major product in the above elimination reaction is:
The alkene formed as a major product in the above elimination reaction is:
- CH2=CH2
Q.
Identify the reagent(s) ‘A’ and condition(s) for the reaction:
A = HCl; Anhydrous AlCl3
A = HCl, ZnCl2
A = Cl2, dark, Anhydrous AlCl3
A = Cl2; UV Light
Q. Which of the following can undergo in Hell-Volhard-Zelinsky Reaction?
- HCOOH
- (CH3)3CCOOH
- C6H5COOH
- (CH3)2CHCOOH
Q. Predict the major product of the following reaction:
And select the major product:
And select the major product:
- None of the above
Q.
The products "A" and "B" formed in above reactions are:
The products "A" and "B" formed in above reactions are:
Q. (a) (CH3)3CCH(OH)CH3conc.H2SO4⟶
(b) (CH3)2CHCH(Br)CH3alc.KOH⟶
Choose the correct statement regarding the given reactions:
(b) (CH3)2CHCH(Br)CH3alc.KOH⟶
Choose the correct statement regarding the given reactions:
- Only (a) gives saytzeff product
- Only (b) gives saytzeff product
- Both (a) and (b) gives saytzeff product
- Both (a) and (b) gives hofmann product
Q. Predict the major product of the following reaction:
And select the major product:
And select the major product:
- None of the above
Q. Ethylamine on treatment with 3 equivalents of methyl iodide, followed by heating with aqueous Ag2O will give ethene as the main product.
- True
- False
Q. Identify the set of reagent/reaction conditions 'X' and 'Y' in the following set reaction:
- X = dilute aqueous NaOH, 20∘C; Y = HBr/acetic acid, 20∘C
- X = concentrated alcoholic NaOH, 80∘C; Y = HBr/acetic acid, 20∘C
- X = dilute aqueous NaOH, 20∘C, Y = Br2/CHCl3, 0∘C
- X = concentrated alcoholic NaOH, 80∘C;Y=Br2/CHCl3, 0∘C
Q.
Identify product 'P'
Identify product 'P'
Q. R - I on reaction with excess NH3 produces :
- All the above
- 1∘ amine
- 2∘ amine
- 3∘ amine
Q. What is meant by ketal? Give an example of reaction(with mechanism) showing its formation.
Q. The final product(s) of the reaction is/are:
- trimethyl amine
- hexa-1, 4-diene
- hexa-1, 5-diene
- hexa-2, 5-diene
Q.
The alkene formed as a major product in the above elimination reaction is:
The alkene formed as a major product in the above elimination reaction is:
- CH2=CH2
Q. Identify the product of the following reaction:
- CH3−CH=CH2
- H2O
- All of these
Q. Identify Z in the reaction sequences.
CH3CH2CH=CH2HBr−−−→H2O2YC2H5OH−−−−−→Z
CH3CH2CH=CH2HBr−−−→H2O2YC2H5OH−−−−−→Z
- CH3(CH2)2CH2−O−C2H5
- (CH3)3CH−O−C2H5
- CH3(CH2)3CH2−O−CH3
- CH3CH2CH(CH3)−O−C2H5
Q. Match the reactions of column I with the reaction mechanisms of column II:
Q.
Which of the following reaction(s) is/are non-stereospecific but stereoselective?
- SN1
- E1
- E2
- E1cB
Q. For the reaction NO2+CO→CO2+NO the experimental rate expression is −dcdt=k[NO2]2 the number of molecules of CO involves in the slowest step will be:
- 0
- 1
- 2
- 3
Q.
Identify product 'P'
Identify product 'P'
Q. Identify the product of the following reaction:
- CH3−CH=CH2
- H2O
- All of these
Q. What do you understand by the term glycosidic linkage?
Q. Predict the major product of the following reaction:
And select the major product:
And select the major product:
- None of the above
Q. Predict the major product of the following reaction:
And select the major product:
And select the major product:
- None of the above
Q. Ethylamine on treatment with 3 equivalents of methyl iodide, followed by heating with aqueous Ag2O will give ethene as the main product.
- True
- False
Q. Hofmann's bromamide reaction is to convert:
- Acid to alcohol
- Alcohol to acid
- Amide to amine
- Amine to amide