Organic Chemistry Fundamentals, IUPAC, Conformations/Stereochemistry (DAT)

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Last updated 9:45 PM on 7/6/26
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59 Terms

1
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Compounds with the same molecular formula but different connectivity of atoms

constitutional isomer

2
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A single bond includes (# sigma/pi) bond(s)

one sigma

3
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A double bond includes (# sigma/pi) bond(s)

one sigma and one pi

4
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A triple bond includes (# sigma/pi) bond(s)

one sigma and two pi

5
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Molecular geometry of NH3

trigonal pyramidal

6
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Molecular geometry of C=C

trigonal planar

7
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In nonpolar solvents, a ___ (shorter/longer) hydrocarbon is more soluble

longer

8
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Acid base reactions favor the formation of ___ acids

weak

9
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Weak acids have a ___ pKa

high

10
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List the carboxylic acid derivatives in order of increasing acidity

amides, ester, ketone, aldehyde, carboxylic acid

11
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EDG ___ (increase/decrease) the acidity of a molecule

decrease

12
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EWG ___ (increase/decrease) the acidity of a molecule

increase

13
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Acronym to remember acidity trends

CARDIO

14
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___ (more/less) positive charge = strong acid

more

15
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___ (large/small) atomic radius = strong acid

large

16
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___ (high/low) electronegativity = strong acid

high

17
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___ (more/less) resonance = strong acid

more

18
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The ___ (more/less) electronegative atoms in a molecule, the more acidic

more

19
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List the orbital hybridization in order of increasing acidity

sp3, sp2, sp

20
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Equilibrium favors the ___ (keto/enol) form

keto

21
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In IUPAC nomenclature, which has higher priority: amide or aldehyde

amide

22
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In IUPAC nomenclature, which has higher priority: ester or ketone

ester

23
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In IUPAC nomenclature, which has higher priority: ketone or aldehyde

aldehyde

24
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In IUPAC nomenclature, which has higher priority: alcohol or ketone

ketone

25
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In IUPAC nomenclature, which has higher priority: alkyne or alkene

alkene

26
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<p>Name the following compound </p>

Name the following compound

spiro[3.4]octane

27
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<p>Name the following compound</p>

Name the following compound

bicyclo[3.3.0]octane

28
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<p>Name the following compound</p>

Name the following compound

cyclohexanecarboxylic acid

29
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<p>Name the following compound</p>

Name the following compound

cyclohexanecarboxamide

30
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List the prefix and suffix for aldehydes

oxo, al

31
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List the prefix and suffix for ketones

oxo, one

32
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List the prefix and suffix for alcohols

hydroxy, ol

33
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List the prefix and suffix for amines

amino, amine

34
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List the prefix for ethers

alkoxy

35
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List the prefix for NO2

nitro

36
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List the suffix for carboxylic acids

oic acid

37
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List the ending word for acid anhydrides

anhydride

38
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List the suffix for esters

oate

39
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List the suffix for acid halides

oyl hallide

40
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List the suffix for amides

amide

41
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List the suffix for nitriles

nitrile

42
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List the prefix and suffix for SH

mercapto, thiol

43
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List the suffix for SO3H

sulfonic acid

44
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List the suffix for sulfides

alkylthio

45
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<p>The common name for this compound</p>

The common name for this compound

acetic acid

46
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<p>The common name for this compound</p>

The common name for this compound

formic acid

47
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<p>The common name for this compound</p>

The common name for this compound

acetone

48
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<p>The common name for this compound</p>

The common name for this compound

formaldehyde

49
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<p>The common name for this compound</p>

The common name for this compound

acetaldehyde

50
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<p>The common name for this compound</p>

The common name for this compound

anisole

51
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<p>The common name for this compound</p>

The common name for this compound

toluene

52
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<p>The common name for this compound</p>

The common name for this compound

styrene

53
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The idea C-C-C bond is ___º

109.5

54
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When a chair is flipped, all substituents pointing up ___ (stay up/become down)

stay up

55
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When a chair is flipped, all axial substituents ___ (stay axial/become equatorial)

become equatorial

56
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These compounds have an internal plane of symmetry

meso

57
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Non-superimposable mirror images that have opposite configuration at all chiral centers

enantiomers

58
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Stereoisomers that are not mirror images; have opposite configuration at some chiral centers

diastereomers

59
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The maximum number of stereoisomers =

2^# chiral centers