Functional Groups Flashcards
alkane general formula
CnH2n+2
alkane general structure
ONLY single bonded carbons
smallest alkane molecule
methane
uses of alkane
combustion reactions
examples of alkanes
mineral oil, petroleum jelly, paraffin max
notable features of alkane
-non-reactive
-non-polar
-hydrophobic
-saturated
- LOWEST BOILING POINT
alkene general formula
CnH2n
alkene general structure
contains at least one double carbon bond
smallest alkene molecule
ethene
uses of alkene molecules
addition reactions
1. alkene + hydrogen –> alkane
2. alkene + water –> alcohol
3. alkene + halogen —> reaction
alkene + hydrogen product?
alkane
alkene + water product?
alcohol
examples of alkenes
plastic (ethene)
notable features of alkene
-non-polar
-reactive
-unsaturated
cis vs tran isomer
- cis = large groups on the same side
- trans = large groups are on opposite sides
alkyne general formula
CnH2n-2
alkyne general structure
contains at least one triple carbon bond
smallest molecule of alkyne
ethyne
uses of alkynes
-ethyne (ripen fruit)
-drugs
notable features of alkynes
-nonpolar
-reactive
-unsaturated
aromatic general structure
compounds made with cyclic rings
smallest molecule of aromatic
benzene
uses of aromatic
-carcinogen (benzene)
-medical antiseptic (phenol)
phenol structure
-OH attached to a benzene ring
notable features of aromatic
-less reactive
-resonance
alcohol general formula
CnH2n+1OH
alcohol general structure
almost the same as an alkane BUT there is an -OH functional group attached
smallest molecule of alcohol
methanol
examples of alcohols
methanol –> formaldehyde
uses of alcohols
-dehydration reaction
-oxidation reactions (alcohol–>carboxylic acids)
notable features of alcohols
-polar
-hydrophobic and hydrophilic part
-flammable
HIGHEST BOILING POINT
ether general structure
R–O–R, oxygen connected to 2 alkyl or aromatic carbons
smallest molecule of an ether
dimethyl ether
examples of ethers
-silkworm (diethyl ether)
-plant oils
-perfumes
notable features of ethers
-very stable
-do not form H-bonds with each other
-break an ether back down using a strong acid (substitution reaction)
thiol general structure
-SH, compounds containing an -SH group
examples of thiols
-protein structure
-curling hair
-repellent (smell)
notable features of thiols
-can be reduced to make disulfide bonds
-functions similar to OH
aldehyde general strucutre
carbonyl group at the end of a chain with a hydrogen
smallest molecule of an aldehyde
formaldehyde
uses of aldehydes
- formaldehyde (antiseptic, embalming)
- acetaldehyde (ripe fruits, narcotic)
notable features of aldehydes
-moderately polar
-H bond with water
-liquid
aldehyde oxidation
-aldehyde —-> primary alcohol
-aldehyde —-> carboxylic acid
ketone general structure
carbonyl group attached to two carbons
smallest molecule of a ketone
acetone (solvent + produced in the liver)
examples of ketone
acetone (solvent + produced in the liver)
notable features of ketones
-moderately polar
-H-bond with water
-liquid
reduction of ketones
ketone —> secondary alcohol
amine general structure
Nitrogen attached to groups
examples of amines
-an amine group + carboxyl acid is in an amino acid
-plants
notable features of an amine
-primary, secondary, tertiary (R bonds)
-weakly basic
basicity of amines
- increase # of lone pairs, higher negative charge, more basic
- decreases conjugation, more basic
carboxylic acid general structure
-COOH group
smallest molecule of carboxylic acid
methanolic acid
examples of carboxylic acids
-acetic acid (vinegar)
-a-hydroxy propanoic acid (lactic acid)
-acetylsalicylic acid (aspirin)
notable features of carboxylic acids
-strong sour odors
-H bonds
-weak acids
esters general structure
-COO, somewhere in the middle of the molecule
examples of esters
flavors and aromas in beer
notable features of esters
-polar
-cannot h-bond
-volatile
amide general structure
Nitrogen bonded to a carbonyl group
notable features of amide
-polar
-can H-bond
-not basic
carboxylic acid + alcohol —>
ester + water
carboxylic acid + ammonia —>
amide + water