null
US
Sign In
Sign Up for Free
Sign Up
We have detected that Javascript is not enabled in your browser. The dynamic nature of our site means that Javascript must be enabled to function properly. Please read our
terms and conditions
for more information.
Next up
Copy and Edit
You need to log in to complete this action!
Register for Free
15973612
Aldehydes and Keytones
Description
Mind Map on Aldehydes and Keytones, created by marcus connolly on 12/11/2018.
No tags specified
carbonyl compounds
oxidation
reduction
a level
Mind Map by
marcus connolly
, updated more than 1 year ago
More
Less
Created by
marcus connolly
about 6 years ago
4
0
0
Resource summary
Aldehydes and Keytones
ALDEHYDES
R-CHO
CnH2nO
Suffix: -al
Functional group is on carbon 1, so don't need to number it
'Proponal'
Reodx Reactions
Oxidiation
Form carboxylic acids
R-CHO + [O] = R-COOH
Primary alcohols are oxidised into aldehydes
R-CH2Oh + [O] = R-CHO + H20
Conditions: Reflux and acidified potassium dichromate
Reduction
Primary alcohols are reduced to aldehydes
R-CHO + 2[H] = R-CH2OH
TESTS
Tollens Reagent
Diamminesilver [Ag(NH3)2]+
Colourless
Produces a grey precipitate or 'silver mirror' if boiled with AG(NH3)2
R-CHO + 2[Ag(NH3)2] + H2O = RCOOH + 2Ag + 4NH3
KEYTONES
R-CO-R'
Suffix: -one
Have to specify where the functional group is
Redox Reactions
Oxidation
Can't be oxidised
Secondary alcohols are oxidised into keytones
R-CH(OH)-R' + [O] = R-CO-R'
Reduction
Reduced into secondary alcohols
R-CO-R' + 2[H] = R-=CH(OH)-R'
Show full summary
Hide full summary
Want to create your own
Mind Maps
for
free
with GoConqr?
Learn more
.
Similar
Oxidation Skills
Robert Hebbs
Organic Chemistry 1 Primer: Lesson II.12
Proton Guru
Redox Reactions
Melissa Lamb
Oxidation number
Ramanathan E
IGCSE Redox Reactions
Jeffrey Piggott
Organic Chemistry 1 Primer: Lesson III.13
Proton Guru
chemistry as level topic 3 redox
Talya Hambling
Organic Chemistry 1 Primer: Lesson III.10
Proton Guru
Organic Chemistry 1 Primer: Lesson II.13
Proton Guru
The blast furnace
Imani :D
NCEA Level 3 Organic Chemistry Reagents
Jayjay Pear
Browse Library