Chem final Flashcards
alkanes alkenes and alkynes at room temp (alky gas)
gas. alkenes and alkynes 1-4 carbons.
benzene names
Methylbenzene is toluene. – Hydroxybenzene is phenol. –
Aminobenzene is aniline.
phenol
benezene w/ OH attached
phenyl
benzene as side chain
do alcohols have high bps?
yes, bc of H bonding
do alkanes have high bps?
no, because they only have london
suffix for alcohols
ol
diols and triols
2 and 3 alcohols
glycols
Diols with two–OH groups on adjacent carbons
if you remove and a O or an H, you almost always have to replace it with…
a double bond
name - O / \ H2C - CH2 (ether) (O but not oxy)
also 4 and 5 (furious diane)
ethylene oxide, and 4 is tetrahydrofuran, and 5 is 1,4 dioxane
alkoxy and ex.
an OR group - OCH3 is methoxy
mercaptan (theo is captain)
thiol - have an SH group
halide common naming
bromide
halide IUPAC naming
1-chloropropane
Configurations (can’t configure the stereo)
Stereoisomers that cannot be converted into one another by rotation around a single bond
formaldehyde (structure) (form JUST ONE)
O
||
H - C - H
acetaldehyde (structure)
O
||
H3C - C - H
common and IUPAC names for ketones
IUPAC name is 3-hexanone. The common name is ethyl propyl ketone
aldehydes and ketones - polar or non?
moderately polar
aldehydes, ketones, amine, acid, amides - soluble or not?
aldehydes, ketones - fewer than five or six carbon atoms are soluble in water because they are able to accept hydrogen bonds
amine up to 6.
acid - up to 4 carbons
amides - low weight
can aldehydes and ketones H bond with each other?
no
aldehydes and ketones - low or high bps?
lower boiling points than alcohols but higher boiling points than alkanes because of dipole-dipole interactions
aldehyde + alcohol =
hemiacetal
D is alpha or beta?
beta
if acid is added to an aldehyde and ketone + alcohol =
acetal. No acid it’s just a hemiacetal
hydrolysis of acetal or ketal causes what?
the formation of hemiacetal or hemiketal and then formation of aldehyde and ketone. The reverse.
COC (O double bond)
ketone
naming amines
N,N dimethyl propylamine - if the branches are different. And the parent is the longer chain
N-methylanaline
anything coming off of the N, even if the N is attached to benzene
bp of amines
higher than alkane, but not higher than OH
amines smell like..
ammonia - strong foul odor
carboxylic acid + alcohol = (ester drinks box alcohol)
ester - the biproduct is H20, so you’re literally just moving the O from H20 to the other O.
hierarchy (CEAA KAT AE AAAHA) (see a cat, ae, ah)
Carboxylic Acids > Esters > Amides > Aldehydes > Ketones > Alcohols > Thiols > Amines > Ethers > Alkenes > Alkynes > Alkyl Halides > Alkanes
uses alpha and beta on carbons when naming (god likes boxes)
carboxylic acid