nomenclature :p (intro to organic) Flashcards

1
Q

define ‘addition reaction’

A

molecule joins an unsaturated molecule –> produces saturated molecule

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2
Q

define ‘elimination reaction’

A

molecule is lost from saturated molecule –> forms unsaturated molecule

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3
Q

define ‘substitution reaction’

(quite obvs tbh)

A

an atom/group replaces another atom/group

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4
Q

define ‘dehydration’

(use big word beginning with e)

A

elimination of water

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5
Q

define ‘hydration’

A

addition of water

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6
Q

define ‘dehydrogenation’

(use big word beginning with e)

A

elimination of hydrogen

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7
Q

define ‘hydrogenation’

A

addition of hydrogen

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8
Q

define ‘hydrolysis’

A

reaction which breaks chemical bonds apart & involves water

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9
Q

define ‘organic chem’

A

study of compounds containing C

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10
Q

define ‘homologous series’

A

= family of compounds with same gen. formula, same functional group and similar chemical properties
* each member of family differs by addition of a CH2 group
* gradual change in physical properties

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11
Q

define ‘functional group’

A

atom/group of atoms responsible for most of the chem. reactions of a molecule

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12
Q

define ‘free radical’

A

species with unpaired electron

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13
Q

define ‘nucleophile’

(NucleOphile –> .ON..)

A

lone pair donor

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14
Q

define ‘electrophile’

(Electrophile –> a..Ep…)

A

lone pair acceptor

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15
Q

define ‘hydrocarbon’

A

molecule containing hydrogen & carbon ONLY

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16
Q

define ‘carbocation’

(not a reaction)

A

+vely charged C ion with 3 cov bonds, not 4

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17
Q

define ‘aliphatic’

A

organic compounds containing C chains & branches with no double bonds

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18
Q

define ‘aromatic’

A

organic compounds with 1+ benzene rings

19
Q

define ‘benzene ring’

A

aromatic func. group –> has ring of 6 C atoms, bonded by alternating single and double bonds

20
Q

define ‘cyclic’

A

organic compounds with C rings (NOT aromatic)

21
Q

define ‘stereoisomerism’

A

molecules with same molecular & structural formulae but diff. spatial arrangement of atoms

22
Q

define ‘geometric isomers’

(type of steroisomerism)

A

diff. arrangement of groups around C=C

23
Q

define ‘optical isomers’

(type of stereoisomerism)

A

molecules = non-superimposable mirror images

24
Q

define ‘structural isomerism’

A

same molecular formula but diff. structure

25
define *'position isomers'* | (type of struc. isomerism)
struc. isomers with func. groups in **diff. positions**
26
define *'functional group isomers'* | (type of structural isomer, dont mix up w. position isomers)
struc. isomers with **diff. functional groups**
27
define *'chain isomers'* | (type of structural isomerism)
struc. isomers with diff. C chain
28
define *'molecular formula'*
gives **actual** no. of atoms of each element in molecule
29
define *'empirical formula'*
gives **simplest** ratio of atoms of each element in molecule
30
define *'general formula'*
* shows no. of atoms of each element in substance, with n C atoms * **all** molecules in homologous series have **same** gen. formula
31
define *'displayed formula'*
shows all bonds & atoms in a molecule eg. H H | --- | C C
32
define *'skeletal formula'*
* lines used to rep. bonds * each vertice = C atom * H atoms **not** shown (unless part of func. group) * other atoms eg. O,N,Cl shown
33
naming carbon chains --> prefixes
* 1C = meth... * 2C = eth... * 3C = prop... * 4C = but... * 5C = pent... * 6C = hex... * 7C = hept... * 8C = oct...
34
rules for naming molecules (from IUPAC)
* count from end of molecule which gives func. group **lowest** no. for its position * always no. position of func. group/double bond before suffix eg. propan-2-ol * func groups take precedence over branched chains when numbering * if <1 diff. func groups, list them in **alphabetical** order (ignore any di/tri..)
35
prefixes to use when there's <1 func. groups
* 2 groups = di... * 3 groups = tri... * 4 groups = tetra... * 5 groups = penta... * 6 groups = hexa...
36
naming ***alkanes***
* single bonds **only** = alkane * molecule has suffix ..ane eg. butane * gen formula = **CnH2n+2**
37
naming ***alkenes***
* contains **double** bond = alkene * molecule has suffix ..ene * gen. formula = **CnH2n**
38
naming ***halogenoalkanes***
* func. group = **-C-halogen** * prefixes for halogen molecules --> > Br = bromo... > Cl = chloro... > F = fluoro... > I = iodo... * gen formula = **CnH(2n+1)X**
39
naming ***alcohols***
* func. group = **O-H** (no double bonds in molecule) * molecule has suffix ...ol (or prefix 'hydroxy' if suffix unusable) * **before** adding suffix, no. of position of O-H on carbon chain
40
naming ***aldehydes***
* func. group = **R-C (//O) (\H)** (where R is C chain, aldehyde group **always** at **end** of molecule) * molecule has suffix ...al
41
naming ***ketones***
* func. group = R - C - R || O (where R is C chain, ketone group **always** in **middle** of molecule) * molecule has suffix ...one (or prefix 'oxo' if suffix unusable)
42
naming ***carboxylic acids***
* func. group = **R-C (//O) (\O-H)** (carboxylic acid group **always** at **end** of molecule) * molecule has suffix ...oic acid
43
naming ***amines***
* func. group = R-NH2 * molecule has suffix ...amine (prefix 'amino' used if suffix can't be used)
44
naming ***nitriles***
* func. group = **R-C =- N** (triple bond) (nitrile group **always** at **end** of molecule) * molecule has suffix ...nitrile