Kaplan Organic Chemistry: Chapter 2 Isomerism Flashcards

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1
Q

name

A

amide

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2
Q

name compound

A

formic acid

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3
Q

name compound

A

acetone

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4
Q

name

A

imine

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5
Q

name

A

imide

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6
Q

name

A

thioether

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7
Q

name

A

sulfoxide

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8
Q

name

A

ether

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9
Q

gauche conformation

A

staggered conformation when 2 largest groups attached to adjacent carbons are only 60 degrees apart.

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10
Q

syn conformation

A

eclipsed conformation when 2 largest groups are interfering with one another

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11
Q

least stable newman projection

A

eclipsed. staggered/anti is the most stable

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12
Q

when can gauche conformation be more stable than anti conformation(when 2 largest groups are 180 degrees apart)?

A

when gauche conformation can allow for intermolecular hydrogen bonds can form.

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13
Q

if the ring has a large substituent, it is more stable if the substituent is ____

A

equitorial- to reduce 1,3, diaxial interactions.

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14
Q

if an atom is facing into the page, it is going ___ on a chair structure. If an atom is facing OUT of the page, it is going ___ on the chair structure.

A

if an atom is facing into the page, it is going DOWN on a chair structure. If an atom is facing OUT of the page, it is going UP on the chair structure.

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15
Q

in Chan-Ingold-Prelog rules, R is ___ and S is ___

A

R is clockwise, S is counterclockwise.

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16
Q

in a fischer projection, verticla lines = ____page, and horizontal lines = ____ page

A

in a fischer projection, verticla lines = INTO page, and horizontal lines = OUT page

VBAC- vertical-back, ( and thus, horizontal, out)

17
Q

Right on fischer = ____ on haworth, left on fischer = ___ on haworth.

A

Right on fischer = DOWN on haworth, left on fischer = UP on haworth.

18
Q

equation for number of stereoisomers

A

2^n

19
Q

configuration differences in enantiomers

A

nonsuperimposable mirror images. will have OPPOSITE configurations from each other (R+S).

20
Q

differences between diastereomers and enantiomers

A

diastereomers are NON mirror images, but are still chiral.

21
Q

epimer

A

a type of diastereomer that differs in absolute config at 1 chiral center.

22
Q

anomer

A

epimers that result from ring close.

23
Q

geometric iosmer

A

diastereomers that differ around a ring OR double bond. cis or trans.

24
Q

T/F: meso compounds are optically active

A

false. meso compounds are not optically active.

25
Q

n is the ___ number. What values can it hold? what PROPERTIES does it denote

A

n= principle number. all positive integers n = 1,2,3..

denotes orbital SIZE and energy LEVEL

26
Q

l is the ___, aka ____ momentum. what values can it be? what property does it denote?

A

l = secondary number aka ANGULAR momentum.

0=s, 1=p, 2=d, 3=f.

the larger the number, the further the electrons get from the nucleus and are easier to eject. the more ā€œsā€ character, the more energy is released when e- gets ejected

properties: orbital shape.

27
Q

why is it harder for an sp hybridized atom to eject an electron than an sp3 hybridized atom

A

the more s character, the closer the e- are to the nucleus, meaning that the electrons are harder to eject because they are mroe drawn.

28
Q

M(l) denotes ___ ____ number. what values can it hold? What property does it denote?

A

Ml denotes the MAGNETIC QUANTUM NUMBER. can range from values of -l to +1. identifies orbial orientation in space.

29
Q

ms is the __ __. What values can it hold? What property does it signify?

A

ms is the SPIN NUMBER. can be +1/2 or -1/2. denotes the electron spin direction.

30
Q

are ketones more polar than alcohols

A

no. alcohols are more polar than ketones because the O is directly bonded to an H.

31
Q

a lewis acid forms ___ __ bonds, where electrons in the bond come from the same starting atom

A

COORDINATE COVALENT.

32
Q

lewis vs bronsted acid

lewis vs bronsted base

A

lewis acid: electron acceptor

lewis base: electron donor

bronsted acid: proton donor

bronsted base: proton acceptor.

33
Q
A