Chapter II Part 2 - Nomenclature Flashcards

(40 cards)

1
Q

2 types of ions

A
  • cat/anionic (met-nonmet)

- polyatomic (comps w/ charge)

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2
Q

how to name ionic compounds w/ fixed neutral charge

KFl

A

no prefixes, bc it’s always in a ratio
last term “-ide”
“Potassium fluoride”

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3
Q

2 types of cov bonds & alt name for “covalent” bonds

A
  • nonmet
  • nonmet & metalloid
    “molecular bonds”
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4
Q

prefixes for cov bonds up to 10

A
mono
di
tri
tetra
penta
hexa
hepta
octo
nona
deca
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5
Q

how do cov bonds end (CO₂)

A

“-ide”

“carbon di-ox-ide”

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6
Q

what charge ion comes first when naming a fixed charge compound (with lithium and flouride)

A

the positive charge

lithium + fluoride –> LiFl

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7
Q

how to name variable charge ions (Fe2+ & Fe3+)

A

roman numerals = ion charge
Fe2+ –> Iron (II) ion
Fe3+ –> Iron (III) ion

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8
Q

Difference between ion & covalent comp ratios

A

Ion ratios = reduced to lowest form, bc in lattice

Covalent ratios = not reduced, bc different ratios make different molecules

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9
Q

define hydrate

A

ion comps bonding to a certain # of water molecules in a crystal lattice

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10
Q

2 steps to name hydrates (ex. MgSO₄ ⋅ 7H₂O)

A

1) Name the ion (“magnesium sulfate”)
2) Take the cov comp prefix that matches the # of molecules of water, & put “hydrate” @ end:
“magnesium sulfate heptahydrate”

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11
Q

how to write form for hydrates (ex. “magnesium sulfate heptahydrate”)

A

1) Write out ion & corresponding # of water molecules
2) Put operator dot between them:
- -> MgSO₄ ⋅ 7H₂O

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12
Q

Define Arrhenius acid

A

compound forming H⁺ hydrogen ions when put in a solution (of water)

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13
Q

4 symbols to use when writing acid reactions

A
g = gas
l = liquid 
s = solid
aq = aqueous (in water)
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14
Q

how to start naming an acid

A

separate the ion from the H+ one, and look at the name of the ion you have

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15
Q

how to name an acid if the ion it forms after H⁺ separation, ends in “-ide”

A

hydro - (ion) - ic acid
“hydrochloric acid”
(chloride ion)

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16
Q

how to name an acid if the ion it forms after H⁺ separation, ends in “-ate”

A

(ion) - ic acid
“sulfuric acid”
(sulfate ion)

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17
Q

how to name an acid if the ion it forms after H⁺ separation, ends in “-ite”

A

(ion) - ous acid
“sulfurous acid”
(sulfite ion)

18
Q

what are all 4 names for that wack compound

A

acetic acid
vinegar
CH₃COOH
HC₂H₃O₂

19
Q

what 2 elements use the whole element name in an acid

A

sulfur & phosphorus

20
Q

what makes up an organic compound

A

most C & H, also other nonmetals

21
Q

3 types of organic hydrocarbons

A

alkanes, alkenes, alkynes

22
Q

alkanes x 3

A
  • single C bonds
  • usually to 4 other atoms
  • end names of comps w/ “-ane”
23
Q

alkenes x 2

A
  • 1+ double C bond

- end names of comps w/ “-ene’

24
Q

alkynes x 2

A
  • 1+ triple C bond

- end names of comps w/ “-yne”

25
Prefixes for organic comps, 1-10
``` meth- eth- prop- but- pent- 6-10 are same as for cov comps ```
26
what are the 3 forms you write organic comps in
- chemical formula - condensed chem formula (structure form in letters & w/o bond lines ig) - expanded-structure form (like how dr. white had you draw)
27
formula for alkane chem forms
CₙH₂ₙ₊₂
28
define cyclo-comps
organic comps w/ c-bonds arranged in a circle
29
formula for cyclo-comp chem forms
CₙH₂ₙ
30
Q. How to write chem form, expand-structure form, & condensed form for smth like propane
1) see propane prefix = "prop" = 3, so 3 C's in the bond 2) see propane suffix = "ane" = alkane = single bonds from c 3) So for structure, put 3 C's together in the bond, & connect them to each other, & enough H's to fill the holes 4) Condensed: take each C & add up each H connected to it, to get bond (CH₃CH₂CH₃ in this case) 5) Chem form: just simplify the condensed form (so C₃H₈ here)
31
def Functional groups x 3
- aka "substituent" groups - atom(s) replacing H in organic comp - used to classify organic comps
32
Alcohol extra group & expanded structure
OH w/ C .....H.....H H--C----C---OH .....H.....H
33
ether extra group & expanded structure
O connected to C on both sides CH₃CH₂ -- O -- CH₂CH₃
34
carbonyl extra group & expanded structure
C center, double bond w/ O ....O .....|| ---C---
35
aldehyde extra group & expanded structure
carbonyl C & 1+ H ...........O ............|| H₃C---C---H
36
ketone extra group & expanded structure
carbonyl connected to 2 C atoms; no H .......O ........|| C---C---C
37
Carboxylic acid extra group & expanded structure
carbonyl + OH ....O .....|| ---C--- OH
38
Ester extra group & expanded structure
carbonyl + ether ....O .....|| ---C---O--C
39
Amine extra group & expanded structure
has N | C - NH₂
40
what does 2-butene mean
the double bond is on the 2nd C in the chain of 5