4.1.1 Basic concepts and hydrocarbons Flashcards

1
Q

hydrocarbon definition

A

contains hydrogen and carbon atoms only

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2
Q

saturated definition

A

contains only carbon-carbon single bonds

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3
Q

unsaturated definition

A

contains carbon-carbon double bonds

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4
Q

molecular formula definition

A

formula which shows the actual number of each type of atom

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5
Q

empirical formula definition

A

simplest whole number ratio of atoms of each element in a compound

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6
Q

general formula definition

A

algebraic formula for a homologous series

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7
Q

structural formula definition

A

minimal detail that shows the arrangement of atoms in a molecule

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8
Q

displayed formula definition

A

shows all the elements and the bonds present within a molecule

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9
Q

skeletal formula definition

A

shows the simplified organic formula by removing any hydrogen atoms from alkyl chains, leaving just a carbon skeleton and associated functional groups

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10
Q

aliphatic definition

A

a compound containing carbon and hydrogen joined together in straight chains, branched chains or
non-aromatic rings

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11
Q

alicyclic definition

A

an aliphatic compound arranged in non-aromatic rings with or without side chains

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12
Q

aromatic definition

A

an aliphatic compound arranged in non-aromatic rings with or without side chains

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13
Q

Homologous series definition

A

families of organic compounds with the same functional group and general formula
they show a gradual change in physical properties
each successive member differs by CH2
same chemical properties

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14
Q

Functional group

A

An atom or group of atoms which when present in different molecules causes them to have similar chemical properties

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15
Q

Alkanes

A

CnH2n+2

Ane

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16
Q

Alkenes

A

CnH2n

Ene

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17
Q

Alcohols

A

OH

Ol or hydroxy

18
Q

Haloalkanes

A

Chloro
Bromo
Iodo

19
Q

Aldehydes

A

C=O at end
al
Formyl

20
Q

Ketones

A

C=O in the middle
one
Oxo

21
Q

Carboxylic acids

A

C=O OH

oic acid

22
Q

Esters

A

C=O O

-yl-oate

23
Q

Order of priority

A
Carboxylic acids
Aldehydes
Ketones
Alcohols
Alkenes
Halogenoalkanes
24
Q

General rule for naming carbon chains

A

Count longest chain and name appropriately
Find any branched chains and count carbons
Add appropriate prefix

25
Alkyl groups
``` Methyl Ethyl Propyl Butyl Pentyl Hexyl ```
26
Naming Alkenes
Double bond between the carbon stakes the number of the lowest carbon it is attached to May have EZ isomers More than one double bond then diene or triene and stem ends in a Suffixes for alkenes can go in front of other suffixes
27
Naming haloalkanes
Prefix fluoro chloro brook iodo
28
Naming alcohols
OH group If di or tri then need e on stem name If alcohol has another group with higher priority then hydroxy-
29
Naming aldehydes
Name ends in al C=O is always on carbon one If two aldehyde groups then di is before al and e is added to stem
30
Naming ketones
End in one | If two ketones then di before one and e is added to stem
31
Naming carboxylic acids
End oic acid | Dioic acid if two
32
Naming esters
Name right to left | yl anoate
33
Define structural isomer
Same molecular formula | Different structural formula
34
How can structural isomers arise
Chain isomerism Position isomerism Functional group isomerism
35
Define homolytic fission
Where each atom gets one electron from the covalent bond
36
When a bond breaks by homolytic fission what forms
2 free radicals
37
Define free radical
Reactive species which possessed an unpaired electron
38
Define heterolytic fission
When a covalent bond breaks and one atom in the share gets both electrons
39
What does heterolytic fission produce
Ions
40
What do curly arrows show
Movement of electron pair showing either breaking or formation of a covalent bond
41
Where do curly arrows start from
A lone pair of electrons or centre of a bond