Brainscape's Knowledge GenomeTM

Browse over 1 million classes created by top students, professors, publishers, and experts.


See full index

A level Chemistry AQA Lewis > 3.3.1 - Introduction to Organic Chemistry > Flashcards

3.3.1 - Introduction to Organic Chemistry Flashcards

You may prefer our related Brainscape-certified flashcards:
AP® Chemistry flashcards Periodic Table flashcards Chemistry 101 flashcards Organic Chemistry 101 flashcards
1
Q

Define General Formula

A

An algebraic formula that can describe any member of a family of compounds

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Define Empirical formula

A

Simplest ratio of atoms of each element in a compound

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Define Molecular formula

A

Actual number of atoms of each element in a molecule

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Define Structural Formula

A

Shows the atoms carbon by carbon + attached hydrogens & functional groups

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Define Skeletal Formula

A

Shows the bonds of the carbon skeleton ONLY + any functional groups

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Define Displayed Formula

A

Shows how all the atoms are arranged and all the bonds between them

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What is the functional group for alkanes?

A

C—C

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What is the functional group for alkenes?

A

C=C

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What is the functional group for alcohols?

A

C—OH

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What is the functional group for haloalkanes?

A

C—halogen

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What is the functional group for aldehydes?

A
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What is the functional group for ketones?

A
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What is the functional group for carboxylic acids?

A
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What is the functional group for nitriles?

A
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What is the functional group for amines?

A
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What is suffix for alkenes?

A

-ene

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

What is suffix & prefix for alcohols?

A

-ol & hydroxy-

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

What is the prefix for haloalkanes? (4x)

A
  • fluoro-
  • chloro-
  • bromo-
  • iodo-
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

What is the suffix for aldehydes?

A

-(an)al

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

What is the prefix & suffix for ketones?

A

oxo- & -(an)one

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

What is the suffix for carboxylic acids?

A

-(an)oic acid

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

What is the suffix for nitriles?

A

-(anen)nitrile

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q

What is the prefix & suffix for amines?

A

-(yl)amine & amino-

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
24
Q

What is the general formula for alkanes?

A

CnH2n+2

(n = 1,2,3 etc.)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
25
Q

What is the general formula for alkenes?

A

CnH2n

(n = 1,2,3 etc.)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
26
Q

What is the general formula for alcohols?

A

CnH2n+1OH

(n = 1,2,3 etc.)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
27
Q

What is the general formula for carboxylic acids?

A

CnH2n+1COOH

(n = 0,1,2 etc.)

28
Q

What is the general formula for haloalkanes?

A

CnH2n+1X

(n = 1,2,3 etc.)

(X = F, Cl etc.)

29
Q

What is the general formula for primary amines?

A

CnH2n+1NH2

(n = 1,2,3 etc.)

30
Q

What is the general formula for aldehydes?

A

CnH2n+1CHO

(n = 0,1,2 etc.)

31
Q

What is the general formula for ketones?

A

CmH2m+1COCnH2n+1

(m & n = 0,1,2 etc.)

32
Q

Name 5 features of a homologous series

A
  1. Chemically similar / react in same way
  2. Each successive member differs by CH2
  3. Same general formula
  4. Same functional group
  5. Gradation in physical properties or specified trend
33
Q

What effect does the length of the carbon chain have on chemical reactivity of the functional group?

A

Has little effect

34
Q

What affects the physical properties (e.g. melting/boiling point & solubility) of carbon molecule?

A

The length of carbon chain

35
Q

In general: small molecules are ___ and larger ones are ____ + _____

A

gas & liquids + solids

36
Q

Why does the length of the carbon chain affect physical properties?

A

Melting/boiling points increase by small amounts as no. of C in chain increases ∵ intermolecular forces increase

37
Q

How does chain branching generally affect melting points and why?

A
  • Reduces melting points
  • ∵ less surface area (molecules pack together less well) & weaker van der Waals forces
38
Q

Hydrogen ring molecules have prefix of ____

A

‘cyclo’

39
Q

What are isomers?

A

Molecules that have the same molecular formula but their atoms are arranged differently

40
Q

Name 2 type of isomers

A

Stereoisomers & structural isomers

41
Q

What are structural isomers?

A

Have same molecular formula but different structural formulas

42
Q

Name 3 types of structural isomers

A
  • Chain Isomers
  • Positional Isomers
  • Functional Group Isomers
43
Q

What is a chain isomer?

A
  • Same molecular formula
  • Hydrocarbon chain is arranged differently
44
Q

What is a positional isomer?

A
  • Compounds with same molecular formula
  • But different structures due to different positions of the same functional group on
  • The same carbon chain
45
Q

What are functional group isomers?

A
  • Same molecular formula
  • Have the same atoms but have different functional groups
46
Q

What are stereoisomers?

A

(Where 2 or more) compounds with the same structural formula but with atoms arranged differently in space

47
Q

_____ show E/Z Isomerism

A

Alkenes

48
Q

The atoms connected to the C=C double bonds _____ rotate around them like they can around single bonds

A

Cannot

49
Q

What causes the type of stereoisomerism called E/Z isomerism?

A

Restricted rotation around the (planar) C=C double bond

50
Q

Explain how alkenes show E/Z isomerism

A
  1. Alkenes have restricted rotation around their C=C double bonds
  2. & if both of the double-bond carbons have different functional groups attached to them = get 2 stereoisomers (E/Z isomerism)
51
Q

Where are the same groups situated in (cis) Z-isomer?

A

Either both above or both below double bond

(matching groups are on ‘ze zame zide’)

52
Q

Where are the same groups situated in (trans) E-isomer?

A

Same groups positioned across the double bond

(matching groups are ‘enemies’)

53
Q

What rules do we use to identify whether a molcule with a C=C bond, surrounded by 3 or 4 different functional groups, is a E- or Z- isomer?

A

Use the Cahn-Ingold-Prelog (CIP) priority rules

54
Q

Describe how we use the CIP rules to identify a E-/Z-isomer

A
  1. Identify the groups directly bonded to each of the C=C carbon atoms
  2. Assign a priority by finding the atom with the highest atomic number - this given the highest priority
  3. If higher priority groups = same side of molecule = Z-isomer OR if higher priority groups = different sides of molecule = E-isomer
55
Q

CIP rules: What do you do if the atoms directly bonded to carbon are the same?

A

Look at next atom in the groups to work out which has the higher priority

56
Q

Why is the IUPAC system used for naming organic compounds?

A

It’s the agreed international language of chemistry so it allows scientific ideas to be communicated across the globe more effectively

57
Q

What are mechanisms?

A

Diagrams that break reactions down into individual stages

58
Q

What reaction do mechanisms show?

A

How molecules react together

59
Q

What do curly arrows show?

A

How electron pairs move around in reactions

60
Q

As electrons are _____ _____, they move from areas of high ______ _____ to more _____ ____ areas

A

As electrons are negatively charged = move from areas of high electron density to more positively charged areas

(e.g. pair of electrons = attracted to carbon atom at positive end of a polar bond)

61
Q

Explain how free radicals form?

A
  1. Sometimes a covalent bond may break in such a way that 1 electron goes to each atom that originally formed the bond
  2. These fragments of original molecule have an unpaired electron = called free radicals
62
Q

Free radicals are extremely ____

A

reactive

63
Q

How are free radicals represented?

A

By a dot

(e.g. CH3• = methyl radical)

64
Q

What is the functional group of an ester?

A

-COO

65
Q

State the name of CH3CH=CHCH2OH

A

But-2-en-1-ol

A level Chemistry AQA Lewis (34 decks)

Brainscape helps you reach your goals faster, through stronger study habits.
© 2024 Bold Learning Solutions. Terms and Conditions