3.3.1 Introduction to Organic Chemistry Flashcards

1
Q

Define General Formula

A

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

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2
Q

Define Empirical formula

A

Simplest ratio of atoms of each element in a compound

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3
Q

Define Molecular formula

A

Actual number of atoms of each element in a molecule

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4
Q

Define Structural Formula

A

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

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5
Q

Define Skeletal Formula

A

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

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6
Q

Define Displayed Formula

A

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

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7
Q

What is the functional group for alkanes?

A

C—C

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8
Q

What is the functional group for alkenes?

A

C=C

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9
Q

What is the functional group for haloalkanes?

A

C—halogen

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10
Q

What is suffix for alkenes?

A

-ene

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11
Q

What is the prefix for haloalkanes? (4x)

A
  • fluoro-
  • chloro-
  • bromo-
  • iodo-
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12
Q

What is the general formula for alkanes?

A

CnH2n+2

(n = 1,2,3 etc.)

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13
Q

What is the general formula for alkenes?

A

CnH2n

(n = 1,2,3 etc.)

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14
Q

What is the general formula for haloalkanes?

A

CnH2n+1X

(n = 1,2,3 etc.)

(X = F, Cl etc.)

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15
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
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16
Q

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

A

Has little effect

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17
Q

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

A

The length of carbon chain

18
Q

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

A

gas & liquids + solids

19
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

20
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
21
Q

Hydrogen ring molecules have prefix of ____

A

‘cyclo’

22
Q

What are isomers?

A

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

23
Q

Name 2 type of isomers

A

Stereoisomers & structural isomers

24
Q

What are structural isomers?

A

Have same molecular formula but different structural formulas

25
Q

Name 3 types of structural isomers

A
  • Chain Isomers
  • Positional Isomers
  • Functional Group Isomers
26
Q

What is a chain isomer?

A
  • Same molecular formula
  • Hydrocarbon chain is arranged differently
27
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
28
Q

What are functional group isomers?

A
  • Same molecular formula
  • Have the same atoms but have different functional groups
29
Q

What are stereoisomers?

A

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

30
Q

_____ show E/Z Isomerism

A

Alkenes

31
Q

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

A

Cannot

32
Q

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

A

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

33
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)
34
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’)

35
Q

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

A

Same groups positioned across the double bond

(matching groups are ‘enemies’)

36
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

37
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
38
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

39
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

40
Q

State the name of CH3CH=CHCH2OH

A

But-2-en-1-ol