Back to marketplace

MD From older spec

No description yet. This curated deck is ready for daily study.

Total cards: 24•Content version: v4•Public deck•Updated: 8/1/2026

Card preview (24)

#1
Front (Question)

Reagents and conditions to convert benzene to sulfonic acid

Back (Answer)

conc. Sulfuric Acid Reflux

#2
Front (Question)

Reagents and conditions to convert benzene to bromobenzene

Back (Answer)

Liquid Bromine FeBr3 catalyst Room Temperature

#3
Front (Question)

Reagents and conditions to convert benzene to cyclohexane

Back (Answer)

(Hydrogenation) Hydrogen gas, 30 atm Finely divided Nickel powder 300 Celcius

#4
Front (Question)

Reagents and conditions to convert benzene to acylbenzene

Back (Answer)

(Friedel-Crafts Acylation) Either Acyl chloride or acid anhydride Reflux AlCl3 catalyst

#5
Front (Question)

Reagents and conditions to convert benzene to alkylbenzene

Back (Answer)

(Friedel-Crafts Alkylation) chloroalkane Reflux AlCl3 catalyst

#6
Front (Question)

Reagents and conditions to convert benzene to nitrobenzene

Back (Answer)

conc. Nitric acid conc. Sulfuric acid For monosubstitution, keep below 55 Celcius

#7
Front (Question)

Reagents and conditions to convert benzene to chlorobenzene

Back (Answer)

Chlorine gas AlCl3 catalyst (Anhydrous, ie, no water present) Room temperature

#8
Front (Question)

Reagents and conditions to convert a primary alcohol to bromoalkane

Back (Answer)

HBr (NaBr + c. sulphuric acid) reflux

#9
Front (Question)

Reagents and conditions to convert a primary alcohol to chloroalkane

Back (Answer)

conc. HCl

#10
Front (Question)

Reagents and conditions to convert a primary alcohol to an alkene

Back (Answer)

Solid aluminium oxide 300 degrees OR c. sulphuric acid reflux

#11
Front (Question)

Reagents and conditions to convert a primary alcohol to an aldehyde

Back (Answer)

Acidified potassium dichromate Distillation

#12
Front (Question)

Reagents and conditions to convert an aldehyde to a carboxylic acid

Back (Answer)

Acidified potassium dichromate reflux

#13
Front (Question)

Reagents and conditions to convert an aldehyde to a primary alcohol

Back (Answer)

NaBH4

#14
Front (Question)

Both sets of reagents and conditions to convert a primary alcohol to an ester

Back (Answer)

1: Acyl chloride OR acid anhydride anhydrous conditions OR 2: Carboxylic acid c. Conc sulphuric acid catalyst reflux

#15
Front (Question)

Reagents and conditions to convert an aldehyde to a carboxylic acid

Back (Answer)

Cr2O72-/H+ (aq) reflux OR Heat with Fehling’s solution

#16
Front (Question)

Reagents and conditions to convert an aldehyde to a cyanohydrin

Back (Answer)

HCN alkaline conditions

#17
Front (Question)

Reagent to convert a carboxylic acid to a carboxylate ion

Back (Answer)

NaOH(aq)

#18
Front (Question)

Reagent for converting a carboxylate ion into a carboxylic acid

Back (Answer)

HCl(aq)

#19
Front (Question)

Reagent and catalyst used for converting a carboxylic acid into an ester

Back (Answer)

An alcohol and concentrated H2SO4 as a catalyst

#20
Front (Question)

Reagents for the conversion of a ketone into a cyanohydrin

Back (Answer)

HCN +alkali

#21
Front (Question)

Reagents for the conversion of a ketone into a secondary alcohol

Back (Answer)

NaBH4

#22
Front (Question)

Conditions and reagents for hydrolysing an ester into a carboxylic acid

Back (Answer)

Reflux with aqueous avid or alkali Using alkali gives the salt of carboxylic acid

#23
Front (Question)

Conditions and reagents for converting an acid anhydride into an ester

Back (Answer)

An alcohol, anhydrous conditions, reflux

#24
Front (Question)

Conditions and reagents for converting an acyl chloride into an ester

Back (Answer)

An alcohol, room temperature