10/10 Flashcards

1
Q

what is a stereoisomer?

A

a compound with the same chemical formula, but a different 3-dimensional arrangement of atoms. ( how they look in space)

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2
Q

Why do we care about stereoisomers?

A

because they can have different effects in the body

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3
Q

Drug companies have to prove to the FDA that a drug being proposed has either: (regarding stereoisomers)

A

single chemical entity, (one version of the stereoisomer) or
prove that both of the stereoisomers in the racemic mixture is safe

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4
Q

what makes up a stereoisomer?

A

stereocenter/chiral center/stereogenic center
and either a enantiomer or diastereomer

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5
Q

where a wedge or dash exists for this class, that is the

A

stereocenter

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6
Q

What are the 2 types of stereoisomers

A

Enantiomers and diastereomers

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7
Q

how do you know when you are dealing with a diastereomers?

A

all of their properties are different. They don’t have a lot incommon except their chemical formula and arrangement of atoms.

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8
Q

what is the one property that is different in an enantiomer?

A

enantiomers are mirror images except for their optical rotation

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9
Q

what is the optical rotation?

A

something that rotates polarized light
left (counterclockwise) is the negative direction
right (clockwise) is the positive direction

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10
Q

in a stereocenter: for carbon atoms that only contain single bonds, there must be ______ different groups attached

A

4

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11
Q

how to denote a stereocenter without a wedge or dash?

A

an asterisck

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12
Q

which direction are solid wedges?
which direction are dashes?

A

in plane groups in: FRONT coming towards you
out of plane groups: BACK going away from you

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13
Q

what are the rules to labeling stereocenters?

A
  1. prioritize the atoms by increasing atomic number (look at the periodic table)
    *if 2 or more are the same, look at what they are attached to to find a point of difference.
  2. Only consider atoms 1-3
    * if it is clockwise (to the right)=R stereoisomer
    * if is it counterclockwise (to the left= S stereoisomer
  3. look at group 4.
    *if it is on the dash, the stereocenter is on the dash, keep it as it is
    *if it is on the wedge, invert the isomer.
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14
Q

hydrogen always has the least ____ when labeling stereocenters

A

priority. The atomic number is 1, nothing is smaller than 1

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15
Q

for carbons in an alkene, there must be two different groups attached to

A

each carbon of the double bond

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16
Q

when labeling stereoisomers on alkenes, what are the naming options?

A

E=opposite side
Z=same side

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17
Q

enantiomers can have 1 or more

A

stereocenters

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18
Q

how to tell if you have an enantiomers in a picture of 2 structures?

A

all the stereocenters must be switched between 2 structures

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19
Q

why can enantiomers impact how a compound interacts within the body?

A

the body recognizes the different stereocenter.

(i.e. spearmint vs. caraway seed smells)

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20
Q

in a diastereomers you have to have a minimum of ____ stereocenters

A

2

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21
Q

how to tell if you have an diastereomers in a picture of 2 structures?

A

one stereocenter changes and one stays the same (dash vs wedge)

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22
Q

diastereomers structures are completely _______

A

different. Can even happen in different physical properties and have a liquid and a solid

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23
Q

Enantiomers isomers usually involves one part that can be dangerous, usually diastereomers match doesn’t really do

A

much of anything

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24
Q

what is the standard aromatic compound?

A

Benzene

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25
Q

heterocycles

A

a ring compound that contains a heteroatom (P, O, N, S)

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26
Q

The benzene ring is very _______

A

stable and common

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27
Q

substituted benzine rings can have different names based on the

A

substituents attached to them

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28
Q

Name this substituted benzene

A

toluene

29
Q

Name this substituted benzene

A

cumene

30
Q

Name this substituted benzene

A

styrene

31
Q

Name this substituted benzene

A

phenol

32
Q

Name this substituted benzene

A

anisole

33
Q

Name this substituted Benzene

A

Aniline

34
Q

Name this di-substituted benzene

A

2-bromotoluene

35
Q

Name this di-substituted benzene

A

3-methylstyrene

36
Q

Name this di-substituted benzene

A

3-methoxyaniline

37
Q

Name this di-substituted benzene

A

4-isopropylphenol

38
Q

Name this fused benzene

A

naphthalene

39
Q

Name this fused benzene

A

anthracene

40
Q

Name this fused benzene

A

phenanthrene

41
Q

Name this fused benzene

A

pyrene

42
Q

name this aromatic ring

A

benzene

43
Q

name this aromatic ring

A

pyrrole

44
Q

name this aromatic ring

A

furan

45
Q

name this aromatic ring

A

thiophene

46
Q

name this aromatic ring

A

imidazole

47
Q

name this aromatic ring

A

pyridine

48
Q

name this aromatic ring

A

pyrimidine

49
Q

name this aromatic ring

A

indole (benzene with a pyrrole)

50
Q

name this heterocycle

A

tetrahydrofuran (husk of corn)

51
Q

name this heterocycle

A

pyrrolidine

52
Q

name this heterocycle

A

tetrahydropyran

53
Q

name this heterocycle

A

piperidine

54
Q

name this heterocycle

A

piperazine

55
Q

name this heterocycle

A

morpholine

56
Q

Prefix of ‘Benz’ is due to the __________

A

benzene ring

57
Q

Prefix of ‘form’ is due to the __________

A

Hydrogen attached to a carbonyl group. Fire ant bite acid.

58
Q

which drug class is this?

A

steroids

59
Q

which drug class is this?

A

quinines

60
Q

which drug class is this?

A

penicillins

61
Q

which drug class is this?

A

barbituates

62
Q

which drug class is this?

A

benzodiazepines

63
Q

which drug class is this?

A

anesthetics

64
Q

which drug class is this?

A

morphines

65
Q

which drug class is this?

A

bensomorphans

66
Q

which drug class is this?

A

phenylpiperidines

67
Q

Name this fused benzine

A

Fullerene AKA bucky Ball

68
Q

steps to labeling an alkene stereoisomer:

A
  1. find the stereocenter. this is where you have a double bond with 2 carbons.
  2. Look at the right side and decide the priority
  3. look at the left and decide the priority
  4. draw a line through the double bond. If the priorities are both on the top or both on the bottom it is a Z isomer.
    If the priorities are on the opposite side then it is an E isomer.