2 Functional Groups and Nomenclature Flashcards

1
Q

what are Alkanes, alkenes, and alkynes

A

a = 1 bond between 2 carbons
e = 2 bonds between 2 C
y = 3 bonds between 2 C

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2
Q

what r aromatic rings

A

functional groups with a ring with alternating single and double bonds

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3
Q

what are alcohols (3 types)

A

functional groups where C is connected to and OH
○ Primary - 1 carbon connected to the C with an OH
○ Secondary - 2 carbons connected to the C with an OH
○ Tertiary - 3 carbons connected to the C with an OH

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4
Q

what are ethers

A

○ Carbon connected to an Oxygen that is connected to another carbon
C-O-C

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5
Q

what are aldehydes

A

○ Carbon is double bonded to an oxygen and connected to an H

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6
Q

what are keytones

A

○ Carbon double bonded to an O and connected to 2 other carbons

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7
Q

what are carboxylic acids

A

○ Carbon double bonded to an oxygen and that carbon also has an OH connected

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8
Q

what is an ester

A

○ Carbon double bonded to an oxygen and is connected to another oxygen that is connected with another carbon
C-O-C=O

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9
Q

what are acid halides

A

○ Carbon double bonded to an oxygen and is connected to a Halogen (Br, Cl, F, I)

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10
Q

what are the intermolecular forces in order or strength

A

○ Electrostatic > H bonding > dipole-dipole > dispersion

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11
Q

what are electrostatic interactions

A

basically ionic bonds, +ve attracted to -ve

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12
Q

what are dipole - dipole interactions

A

Partial +ve is attracted to partial -ve (dipoles)

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13
Q

what is H bonding

A

○ Partial +ve H atom is attached to a heteroatom, with the partial -ve being on another heteroatom (any atom that is not carbon or hydrogen in organic chemistry)

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14
Q

TF Molecs with a lone pair on an electronegative heteroatom are H bond acceptors

A

T

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15
Q

what are dispersion forces

A

Temporary and instantaneous dipole that forms in molecs
○ Theres a shift in the electron cloud that creates a dipole

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16
Q

TF - If theres a nearby atom or molec it can be influenced to also create a temp dipole

A

T

17
Q

TF molecs prefer solvents with different intermolecular forces

A

F, prefer solvents with similar intermolecular forces “like dissolves like”

18
Q

what does protic and aprotic mean

A

protic = can donate an H bond
aprotic = cant donate and H bond

19
Q

which 2 parameters are solvents classified under

A

Polar + non polar
protic + aprotic

20
Q

TF Something is aprotic if it doesn’t have acidic protons (protons with a partial +ve charge)

A

T

21
Q

Anything that increases electrostatic and dipole interactions, increases ______

A

hydrophilicity

22
Q

Anything that decreases dispersion increases _______

A

hydrophilicity

23
Q

TF more condensed structures have a lower solubility

A

F, higher solubility

24
Q

what are the 3 portions of nomenclature

A
  • A prefix (details about the substituents
  • A root name (how many Cs in the chain / any alkenes or alkynes)
  • A suffix (details about the highest priority functional group
25
Q

what do we do when we have multiple substituents in naming

A

name them in alphabetical order

26
Q

higher priority substituent groups get the ______ number

A

smaller

27
Q

if the compound were naming is a ring we start with _____

A

cyclo

28
Q

when naming compounds, more bonds between carbons means that

A

they are higher priority and well be at the suffix (ene trumps ane)

29
Q

the only thing lower priority than Alk(a/e/y)nes are ____

A

Halides

30
Q

General overview of the naming

A

alphabetical order { location of atom(#) } {(how many Atoms there are)(“Name” of atom) } {Shape of chain if there, then # of carbons} {location of dbl or triple bond if there} {name bond (ane, ene, yne)} {# highest priority thing, then suffix of it}