chem: Add nitriles
This commit is contained in:
parent
e4184f54b0
commit
ae79af4dfa
@ -2,8 +2,6 @@
|
|||||||
|
|
||||||
The course code for this page is **SNC4MZ**.
|
The course code for this page is **SNC4MZ**.
|
||||||
|
|
||||||
CHEM!
|
|
||||||
|
|
||||||
## Organic chemistry
|
## Organic chemistry
|
||||||
|
|
||||||
!!! definition
|
!!! definition
|
||||||
@ -654,6 +652,31 @@ Amides carry the suffix **-amide** and are otherwise named equivalently to ester
|
|||||||
!!! example
|
!!! example
|
||||||
<img src="/resources/images/amide-names.png" width=700>(Source: Kognity)</img>
|
<img src="/resources/images/amide-names.png" width=700>(Source: Kognity)</img>
|
||||||
|
|
||||||
|
### Nitriles
|
||||||
|
|
||||||
|
Nitriles consist of a cyanide(s) attached at the end of a carbon chain.
|
||||||
|
|
||||||
|
$$\ce{R-C#N}$$
|
||||||
|
|
||||||
|
As they can only be placed at the end of a carbon chain, a positional number is not used. These have the highest priority of all organic compounds and use the suffix **-nitrile** and the prefix **cyano-**.
|
||||||
|
|
||||||
|
!!! example
|
||||||
|
- methanenitrile
|
||||||
|
- methanedinitrile
|
||||||
|
|
||||||
|
Nitriles are synthesised through the nucleophilic substitution of halogenoalkanes, **extending their carbon chain**.
|
||||||
|
$$\ce{R-X + C#N- -> R-C#N + X-}$$
|
||||||
|
|
||||||
|
### Reduction reactions
|
||||||
|
|
||||||
|
### Retro-synthesis
|
||||||
|
|
||||||
|
### Simple polymers
|
||||||
|
|
||||||
|
### Polyesters and polyamides
|
||||||
|
|
||||||
|
### Stereoisomers
|
||||||
|
|
||||||
### Properties of organic compounds
|
### Properties of organic compounds
|
||||||
|
|
||||||
**Alcohols** are able to form hydrogen bonds, so are soluble in water. Increasing the length of the main chain decreases solubility as the rest of the molecule is non-polar, but this can be compensated by adding more hydroxyls too.
|
**Alcohols** are able to form hydrogen bonds, so are soluble in water. Increasing the length of the main chain decreases solubility as the rest of the molecule is non-polar, but this can be compensated by adding more hydroxyls too.
|
||||||
|
Loading…
Reference in New Issue
Block a user