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carbonyl chemistry

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Total cards: 21•Content version: v4•Public deck•Updated: 8/1/2026

Card preview (21)

#1
Front (Question)

what is the reagent to test for alkenes and positive test

Back (Answer)

bromine water, decolourises bromine water

#2
Front (Question)

what is the test for a carboxylic and positive test

Back (Answer)

Na2CO3 - carbonate will see fizzing, CO2 gas produced

#3
Front (Question)

what is the test for a primary/secondary alcohol

Back (Answer)

H+/Cr2O7 orange —-> green

#4
Front (Question)

what is the test for phenol and positive test

Back (Answer)

universal indicator and Na2CO3, red —> orange, no fizzing (weak acid)

#5
Front (Question)

what is the test for a haloalkane and positive test

Back (Answer)

AgNO3 (aq) cl- white precipitate br - cream precipitate I - yellow precipitate

#6
Front (Question)

what is test for a Carbonyls ( aldehyde and ketone) and positive test

Back (Answer)

2,4 DNP orange precipitate forms

#7
Front (Question)

What is test for an aldehyde and positive test. what is half equation for formation of Ag

Back (Answer)

Tollens reagent (oxidation reaction) produces a silver mirror. Ag + e- —> Ag (s)

#8
Front (Question)

what reagent should be used to turn an aldehyde/ketone back to a primary alcohol/secondary alcohol, what type of reaction is this, what type of mechanism

Back (Answer)

reagent: aqueous sodium borohydride, NaBH4 this is a reduction reaction nucleophilic addition

#9
Front (Question)

what is a nucleophile

Back (Answer)

donates a pair of electrons

#10
Front (Question)

what is the reagent needed to turn a carbonyl to a hydroxynitrile, (alcohol and CN group ) what is the mechanism

Back (Answer)

H+/NaCN nucleophillic addition

#11
Front (Question)

2,4 DNP is added to an aldehyde or ketone an orange precipitate forms, how this be used to identify the specific compound

Back (Answer)

• recrystallise and dry the precipitate • measure the melting point • compare to known values

#12
Front (Question)

what are the 2 properties of carboxylic acids

Back (Answer)

dissolve in water acids

#13
Front (Question)

why are carboxylic acids soluble in water

Back (Answer)

They can form hydrogen bonds to water molecules

#14
Front (Question)

why are carboxylic acids classed as acids

Back (Answer)

they can donate H+ ions, only weak acids though

#15
Front (Question)

what do carboxylic acids need to react with to make esters. What small product is formed

Back (Answer)

alcohol conc H2SO4 H2O

#16
Front (Question)

What 2 molecules are needed to make an acid anhydride, what small product is formed, what catalyst is needed

Back (Answer)

2 identical carboxylic acids H2O conc H2SO4

#17
Front (Question)

what does an acid anhydride need to react with to make an ester, what other product is made

Back (Answer)

react with an alcohol makes a carboxylic acid

#18
Front (Question)

Esters can be broken down by acid hydrolysis, what reagents are needed, what 2 products are made

Back (Answer)

H+/H20, (reflux) alcohol and carboxylic acid

#19
Front (Question)

esters can also be broken down by alkali hydrolysis, what reagent is needed, what 2 products are made

Back (Answer)

NaOH (reflux) alcohol and carboxylate salt

#20
Front (Question)

How are acyl chlorides made, what is the reagent, what products are made

Back (Answer)

reacting a carboxylic acid with SOCl2 forms SO2 and HCl

#21
Front (Question)

how do acyl chlorides react

Back (Answer)

the -Cl is replaced by a nucleophile which loses one H. HCl is always made.