Decarboxylation
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- The final product is Salicylic acid
- CO2 acts as an electrophile
- Acidification of phenol leads to formation of main product
- Phenoxide ion undergoes electrophilic attack
- 2-chloro-1-nitrobenzene
- 3-nitrochlorobenzene
- 4-chloro-1-nitrobenzene
- equal amounts of (A) and (C)
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What is the conjugate acid of ?
Assertion: Acetic acid does not undergo a haloform reaction.
Reason: Acetic acid has no alpha hydrogen atoms.
The assertion is true, but the Reason is false.
Both Assertion and Reason are false.
Both Assertion and Reason are true. The reason is the correct explanation of the Assertion.
Both Assertion and Reason are true. The reason is not the correct explanation for Assertion.
- Reduction of acyl halide through Na/C2H5OH
- Reduction of ester through Na/C2H5OH
- Reduction of anhydride through Na/C2H5OH
- Reduction of carbonyl compounds through Na/C2H5OH
- 142
- 124
- 130
- 122
- CH3O−/CH3CH2OH
- CH3O−/acetone
- (CH3)3C−O−/butyl alcohol
- All of the above
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CRON
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- Hexachlorobenzene
- Hexachlorocyclohexane
- 2, 4, 6−Trichlorophenol
- 1, 4−Dichlorobenzene
Name an acid that is solid at room temperature.
- IV > II > III > I
- III > II > I > IV
- I > II > III > IV
- IV > III > II > I
- Rate of sulphonation for C6H6 is higher than C6D6
- On treatment of salicylic acid with Br2/H2O (in excess), it results in a dibromo product
- When HCOOEt is treated with MeMgBr in excess followed by hydrolysis, it will result in the formation of tertiary alcohol
Products formed is a pair of enantiomer
Which of the above compounds reacts with NaHCO3 to give CO2?
- I, II and III
- I and III
- II and III
- I and II
- 2
- 3
- 4
- 5
Predict the natue of [X] & [Y] in the above reaction.
Schemes and describe the conversion of P to Q a
nd R to S, respectively. Scheme describes the synthesis of T from Q and S. The total number of atoms in a molecule of T is_______
(B) \( \frac{\text { (i) } CHCl _{3}, NaOH }{\text { (ii) } H _{3} O ^{+}} \) \( \frac{ Br _{2} \text { in } CS _{2}}{273 K } \rightarrow \) (A)