ochem Flashcards
priority
functional, double/triple bonds, substituents (phenol, ethyl, methyl, chloro)
carboxylic acid
ester
amide
aldehyde
ketone
alchohol
amine
alkene
alkyne
alkane
ether
alkyl halide
organic chemistry is
the study of the structure and physical and chemical properties of organic compounds
aliphatic vs aromatic
aliphatic- linear branched or ring chains of Carbon atoms
aromatic- closed rings of carbon atoms based on benzene
saturated hydrocarbons vs unsaturated hydrocarbons
saturated- max number of H
unsaturated- non-max number of H
alkane characteristics
- non polar covalent bonds and the forces between alkanes r weak
- insoluble in water
alkyl group
1+ carbon atoms that form a branch off the main chain of a hydrocarbon, type of substituent group that replaced hydrogen
structural isomers
same molecular formula, different arrangement
- for any isomers
iso__ane (delete one carbon, and replace on hydrogen on the centre carbon with a methyl group)
do the same but with 2 methyl groups
alkenes definition
- aliphatic hydrocarbons with at least one C=C (unsaturated)
alkenes characteristics
physical:
boiling point is less than a similar sized alkane
- insoluble in water (non polar)
chemical:
- relatively high reactivity
- can undergo combustion reaction
- can undergo substitution reaction
- undergo polymerization reaction
alkynes characteristics
- aliphatic hydrocarbons with molecules containing at least 1 C triple C
- similar properties to alkenes
stereoisomer
- same kind and number of atoms bonded in the same order but different arrangements in space
- cannot be charged from one to another by simple rotation
- distinct compounds with different properties, such as diff melting points
can C=C bonds rotate?
no, which is how we get cis and trans bonds
ketones are substiutients are named as
oxo-
properties of aldehydes and ketones
- polar bond between carbon and oxygen
- polar molecule: LDF: dipole dipole
- more soluble in water than alkanes but less than alcohols, solubility in water decreases as the number of carbon increases
properties of carboxylic acid
- polar molecules due to the C=O and -OH (allows for H bonds), 2 polar groups
- high melting and boiling points
- similar solubility to alcohols
- properties are influenced by the length of the carbon change
- weak acids
esters
- carboxyl where the H atom is subbed in by an alkyl group
properties of esters
- similar melting and boiling points to aldehydes and ketones of similar size
- smaller esters are gases; larger are waxy solids
- compared to carboxylic acids
- less polar: due to the lack of -OH
- less soluble in water, lower boiling point
properties of amines
- small amines are soluble in water
- N-C and N-H bonds are polar
- boiling points and melting points are higher than that of hydrocarbons
- boiling points of primary amines is higher than secondary which is higher than tertiary bc of the lack of H bonds
properties of amides
- primary amides have higher boiling points and melting points than similar amides
- likely due to more H bonds between primary amides
- smaller amides are somewhat soluble in water: -NH groups form H bonds with water, as length of carbon chain increases, solubility decreases
properties of alcohols
- much higher boiling point than that of similarly charged alkanes
- increased polarity due to OH
- IMF: LDF, D-D, H bonds
- smaller alcohols are most soluble in polar compounds
- long chain alcohols w/ long chain carbons let it dissolve in p and np
primary, secondary, tertiary alcohols
primary: attached to one other C
secondary: attached to two other C
tertiary: attached to three other C
less alkyl groups means that primary alcohols have a higher MP and BP
properties of ethers
have polar C-O bonds and the bent structure around C-O-C
- more polar than alkanes but don’t H+ bonds
- BP are higher than alkanes but lower than alcohols
- good organic solvents, has polar and non polar properties
thiols
lower bp than OH
physical properties of hydrocarbons
- alkanes low mp and bp
- alkenes and alkynes have lower mp and bp than alkanes
- bp and mp related to the size: bigger size means more LDF interactions
- all hydrocarbons are non polar, insoluble in water, liquid forms are soluble with other np ones