CHEM 102: Amines and Amides
49 Cards in this Set
Front | Back |
---|---|
What are amines a derivative of?
|
Ammonia (NH3)
|
How do you name amines? (IUPAC)
|
replace the "e"i n alkane to "-amine"
|
When do you number amines to show the position of the -NH2 group and other substituents?
|
When an amine has a chain of 3+ Carbon atoms
|
Name this Amine:
CH3-CH2-CH2-CH2-N-CH3
|
H
|
N-methyl-1-butanamine
|
What classification is this amine? CH3-CH2-CH2-NH2
|
Primary
|
What classification is this amine?
|
Tetriary
|
For the priority of functional groups in IUPAC names Does a carboxylic acid, amide, or ester have the highest priority?
|
Amide<Ester<Carboxylic Acid
|
For the priority of functional groups in IUPAC names does an amide, ketone or aldehyde have the highest priority?
|
ketone<aldehyde<amide
|
For the priority of functional groups in IUPAC names which has the highest priority, alcohol, ketone, or amine?
|
amine<alcohol<ketone
|
For the priority of functional groups in IUPAC names halide, alkane, or amine?
|
halide<alkane<amine
|
which has a higher priority, ester or an alcohol?
|
ester
|
which has the lowest priority, alcohol or carboxylic acid?
|
alcohol
|
What is the amine of benzene called?
|
an aniline
|
name this aniline
|
N,N-dimethylaniline
|
Why must there always be 3 H attached to the N in amines?
|
Why must there always be 3 H attached to the N in amines?
|
Why are the Hydrogen bonds of amines weaker than those found in alcohols?
|
Because nitrogen is not as electronegative as oxygen, so the bond are weaker
|
Are N-H bonds polar or non polar?
|
polar, this makes it so that primary and secondary amines can form hydrogen bonds with water
|
What is the common name for this amine?
CH3-CH2-NH2
|
ethyl amine
|
What is the common name for this amine?
CH3
|
CH3-N-CH3
|
trimethylamine
|
How does hydrogen bonding effect primary amines?
|
They have a higher boiling point than secondary amines
|
Why do tertiary amines have the lowest boiling point of the three?
|
because it's not possible for another hydrogen bond to form since there are already 3 present.
|
Are amines solubil in water?
|
Yes, primary are the most soluable, tetriary are the least
|
Do amines react as acids or bases in water?
|
Bases (they are weak though), the lone pair of electrons on the N (because there's an extra space, only 3 Hs are residence, there is a vacancy) is receptive and takes one of the H's from the water. The biproduct in this sort of a reaction is Hydroxide (OH-) (that's what happens to the lef…
|
How is an amine salt formed?
|
when an amine is neutralized by an acid
|
How do you name an amine salt?
|
by replacing "-amine" with "-amonium" followed by the name of the negative ion
|
What are the physical properties of amine salts?
|
ionoic compounds, solid at room temp, soluble in water
|
What illegal drug is an amine salt?
|
cocaine
|
What are examples of heterocyclic amines?
|
DNA and RNA
|
what is a heterocyclic amine?
|
a cyclic amine with a ring of five or six atoms, one or two of them are nitrogen
|
What are alkaloids?
|
physiologically active nitrogen-containing compounds produced by plants
They are used as stimulants, anesthetics, and antidepressants and are often habit forming
|
Common alkaloids mentioned in the slides:
|
Nicotine
Caffeine
|
Amidation: How are amides prepared?
|
by heating a carboxylic acid with ammonia or an amine
|
How do you name amides IUPAC
|
drop the "-ic acid" and add "-amide"
|
what are amides made of?
|
an amino group that replaces the -OH in a carboxylic acid
|
What is the name for this amide?
CH3-Ch2_Ch2-CO-NH-CH3
|
n-ethylbutanamide
|
what is the name for this amide?
CH3-CH2-Ch2-Ch2-CO-N-CH2-CH3
|
CH2-Ch3
|
n,n-diethylpentanamide
|
What isthe amide of benzene called?
|
Benzamide
|
Name this amide:
Ch3-Ch2-CH2-Ch2-CO-NH2
|
pentanamide
|
Name this amide:
Ch3-Ch2-Ch2-CO-NH-CH3
|
N-methylbutyramide
|
what does hydrolysis mean?
|
water separation
|
when does hydrolysis occur?
|
when water reacts with an amide in the presence of an acid or a base
|
Amides that undergo acid hydrolysis form
|
carboxylic acid and an amonium salt
|
amides that undergo base hydrolysis form
|
a salt of carboxylic acid and an amine or ammonia
|
What does the hydrolysis of n-ethylpropanamide with NaOH form
|
O
||
CH3CH2CO– Na+ + CH3CH2NH2
|
what does a neurotransmitter do?
|
It's a chemical compound that transmits an impulse from a nerve cell to a target cell
|
What does dopamine do?
|
it's produced in the nerve cells of the midbrain and acts as a natural stimulant to give energy and feeling of enjoyment
|
what does norephinephrine and epinephrine do?
|
they are hormonal neurotransmitters that plan a role in sleep, attention, focus, and alertness
|
What is serotonin's job?
|
to help relax, and sleep deeply, peacefully, think rationally, and provides a wellbeing feeling and calmness
|
What does hte hydrolysis of n-ethylpropanamide with HCl form?
|
propanoic acid (propionic acid) and ethylammonium chloride.
|