14 - introduction to organic chemistry Flashcards

1
Q

ways of representing organic molecules:

A

. empirical formula
. molecular formula
. structural formula
. displayed formula
. skeletal formula

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2
Q

empirical formula

A

simplest ratio of the different types of atoms present in the molecule

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3
Q

molecular formula

A

shows actual numbers of each type of atom in a molecule

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4
Q

structural formula

A

the formula that shows how many, and the symbols of, atoms bonded to each carbon atom in an organic molecule

shows double bonds

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5
Q

displayed formula

A

a 2D representation of an organic molecule, showing all its atoms (by symbols) and their bonds

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6
Q

skeletal formula

A

simplified displayed formula with all C and H atoms and C-H bonds removed

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7
Q

homologous series

A

a group of organic compounds having the same functional group, the same general formula, and similar chemical properties

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8
Q

functional group

A

an atom or group of atoms in an organic molecule which determines the characteristic chemical reactions

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9
Q

general formula

A

a formula that represents a homologous series of compounds using letters and numbers

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10
Q

aliphatic

A

straight or branched chain organic compounds, and also include cyclic organic compounds that do not contain benzene rings

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11
Q

alkenes general formula

A

CnH2n

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12
Q

halogenoalkenes general formula

A

CnH2n+1X

X = F, Cl, Br, I
chloromethane (CH3Cl)

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13
Q

alcohols general formula

A

CnH2n+1OH
methanol (CH3OH)

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14
Q

aldehydes general formula

A

CnHn+1CHO
ethanal (CH3CHO)

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15
Q

ketones general formula

A

CnH2n+1COCmH2m+1
propanone (CH3COCH3)

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16
Q

carboxylic acids general formula

A

CnH2n+1COOH
ethanoic acid (CH3COOH)

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17
Q

esters general formula

A

CnH2n+1COOCmH2m+1
propyl ethanoate (CH3COOC3H7)

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18
Q

amines general formula

A

CnH2n+1NH2
methylamine (CH3NH2)

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19
Q

nitriles general formula

A

CnH2n+1CN
ethanenitrile (CH3CN)

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20
Q

aryl compound

A

have a benzene ring

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21
Q

benzene

A

C6H6 (circle inside hexagon)

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22
Q

single covalent bonds

A

a bond made up of a pair of electrons shared between two atoms

23
Q

sigma bonds

A

a single covalent bond formed by thr end on overlap of atomic orbitals

24
Q

pi bond

A

covalent bond formedc by sideways overlap of p and p OR p and d atomic orbitals

25
why do the two lobes making up a pi bond lie above and below the plane of atoms
to maximise overlap
26
triple bond has how many pi bonds
2
27
structural isomerism
compounds with the same molecular formula but different structural formulae
28
types of structural isomerism
. position isomerism . functional group isomerism . chain isomerism
29
position isomerism
functional group location varies
30
functional group isomerism
different functional groups
31
chain isomerism
different carbon skeleton
32
stereoisomers
compounds whose molecules have the same atoms bonded to each other in the same way, butg with a different arrangement of atoms in space so that the molecules cannot be superimposed by each other
33
types of stereoisomers
. geometrical (cis/trans) isomerism . optical isomerism
34
geometrical (cis/trans) isomerism
. no free rotation about a CC double bond . cis = Br aoms on same side . trans = Br positioned across double bond . have different chemical properties (reaction rates) . possible in substituted cyclic compounds
35
optical isomerism
. also called enantiomers (pair of optically active molecules whose mirror images cannot be superimposed) . C atoms at enantiomers' center is called chiral center . pair of optical rotates a plane polarised light my same magnitude, in opposite directions
36
chiral center
a carbon atom with the four different atoms or group of atoms attached, allows optical isomers to exist
37
do symmetrical substituted cyclic molecules have a chiral center
no
38
reaction mechanism
the series of steps that take place in the course of the overall reaction
39
ways in which a covalent bonds can break
. homolytic fission . heterolytic fission
40
homolytic fission
. both atoms get one electron from the shared covalent pair . make free radicals (shown with a dot) . free radical reaction occurs
41
free radical reaction
. initiation : free radicals formed . propagation : steps regenerating more free radicals . termination : 2 free radicals meet and form a product molecule
42
heterolytic fission
. uneven breaking of a covalent bond . more electrongative atom grakesxc both electrons . forms ions . draw arrow from bond to negative
43
carbocation
an alkyl group with a single positive charge on one of its carbon atoms, formed in reaction mechanisms types: - primary - secondary - tertiary (most stable)
44
inductive effect
the uneven sharing of electrons along a covalent bond, electron donating species are said to have a positive inducing effect
45
more alkyl groups =? stable
more stable
46
more alkyl groups =? stable
more stable
47
electrophile
a species in organic chemistry that cafbm ct as an electron pair acceptor
48
nucleophiles
species that can act as a donor of a pair of electrons
49
types of organic reactions
. addition . elimination . condesnation . substitution reactions (free radical sub) . oxidation . reduction
50
addition reactions
an organic reaction in which two or more molecules combine to give a single product molecule
51
elimination reaction
a reaction in which a small molecule (water, HCl) is removed from an organic molecule
52
condensation reaction
a reaction in which two organic molecules join together and in the process, eliminate a small molecule
53
substitution reaction
a reaction that involve the replacement of one atom or group of atoms, by another