Title | Amines Notes (organic chemistry) |
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Author | Tolu Oware |
Course | Chemistry |
Institution | High School - Canada |
Pages | 2 |
File Size | 87.5 KB |
File Type | |
Total Downloads | 98 |
Total Views | 173 |
Amines Notes...
Amines An amine can be identified by the presence od an amino group -NH2 (ammonia group minus 1 H) whenrein one H has been replaced by an alkyl group. Amines can b classified into primary (1alkyl group, 2 H’s), secondary (2 alkyl groups, one H), and tertiary (3 alkyl groups, no H’s) amines depending on how many alkyl groups replace H atoms. Nomenclature 1. naming amines can be confusing because there are many accepter variations. See eg. A) 2. amines are named as alkanamines. The -e in the alkane name of the longest chain is changed to -amine 3. the chain is numbered to locate the amine group substituents. 4. in a secondary and tertiary amine, the longest chain is numbered. 5. each alkyl group bonded to the N atom is named N-alkyl group. 6. Multiple amines groups are called diamine, triamine etc. 7. when found in compounds with higher priority functional groups (especially O containing functional groups): name the amine group as a substituent (amino). -NH2 : amino-NHR: N-alkylamino-NR2: N,N-dialkylamino-
ANILINE: a common defining molecule. Properties of Amines: Characteristic Higher boiling points than the P hydrocarbon parent chains. Lower melting and boiling points than alcohols of similar molecular weight
Reason olarity of C-N and N-H bonds cause greater intermolecular forces. OH to form H bonds and larger intermolecular forces than N-H bonds
Typically have “Fishy” odours Commonly found in biological proteins and other molecules.
How amines are prepared: Reaction of alkyl halides with ammonia (weak base)
alkylhalide + ammonia amine + hydrogen halide Just like substitution reactions of alkanes with halogens, secondary and tertiary amines can be prod. if the rxn is allowed to continue (more H atoms will be replaced w/ alkyl groups)...