Chapter 6 --organic Chemistry Flashcards

1
Q

Functional group

A

In a molecule is an atom or group of atoms that gives the compound some distinctive and predictable properties

Eg. COOH - gives molecules a sour acidic taste

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2
Q

Homologous series

A

Set of compounds with the same functional group, similar chemical properties and physical properties - show graduation / gradual change from one to the next

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3
Q

Alcohols

A

-OH

ol ending for hydroxyl group

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4
Q

Chain isomerism

A

Structural isomerism

Same molecular formular but different structure eg

CH3-CH2-CH2-CH3

CH3-CH-CH3
|
CH3

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5
Q

Position isomerism

A

Molecules with same functional group but attached in different positions on the same carbon chain

Eg. propan-1-ol , propan-2-ol

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6
Q

Stereoisomerism

A

Have same molecular formular

Same structural formular

Different arrangement

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7
Q

Fractional distillation

A

Converts crude oil into a small number of fractions

Done in a distillation Column

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8
Q

Cracking

A

Demand for shorter chained hydrocarbons is higher.

Passing hydrocarbons in heavier fractions through a heated catalyst (zeolite usually — which is aluminium,silicon, oxygen)
One large molecule —> at least two smaller molecules

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9
Q

Reforming

A

Straight chained allanes burn less efficiently than branches chained /rings (cyclic compounds)

Converts straight chained alkanes into branched/cyclic hydrocarbons by heating them with a catalyst (platinum)
Helps them burn more smoothly in the engine

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10
Q

Inside catalytic converters

A

2CO + O2 —> 2CO2

2NO + 2CO —> N2+2CO2

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11
Q

Biodiesel

A

Vegetable oils

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12
Q

Bioethanol

A

Bacteria made rather than enzymes —- eg corn

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13
Q

Comparing fuels 4

A

Land use
Yield / speed
Manufacture n transport
Carbon neutrality

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14
Q

Radical

A

Species with an unpaired electron

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15
Q

Mechanism

A

Sequence of two or more steps (with each, an equation) that shows how a reaction takes place

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16
Q

Test for Alkene

A

Decolourises bromine water

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17
Q

Hydration catalyst

A

Phosphoric Acod

H3PO4

18
Q

Diol

A

Compound containing two -OH groups

19
Q

Oxidation to diols

A

Oxidising agent - potassium manganate(VII)

Acidic conditions (usually dilute sulfúrico acid)

Potassium manganate(VII) provides oxygen atom and water in solution provides another and 2* Hydrogen atoms

KManganate from purple to colourless (can be used like bromine water to test for alkene)

20
Q

Ketone

A

When a secondary alcohol is oxidised - homologous series

21
Q

Ketone formula

22
Q

Aldehyde

A

When a primary alcohol is oxidised

23
Q

Aldehyde formula

24
Q

Aldehyde oxidised further

A

Gain of oxygen atom not loss of hydrogen

Carboxylic acid

25
Carboxylic acid formula
RCOOH
26
Usual reagent for oxidation reactions primary and secondary alcohols
Mixture of potassium dichromate(VI) and dilute sulfúric acid
27
Ketone ending
-one
28
Aldehyde ending
-al
29
Heating under reflux
When oxidation intended to be complete Products stay in reaction ( boil off but condense in vertical condenser n return to heating flask)
30
Distillation with addition
When oxidation intended to be incomplete - to obtain an aldehyde- Only oxidising agent heated and alcohol slowly added to oxidising agent Aldehyde distils off immediately when formed as has much lower boiling point than alcohol used to make it - aldehyde collected in reciever
31
Why thermometer in distillation
If temp remains steady then indicates one compound is distilling over If temp rises after a while , indicates a diff compound is distilling over
32
Pros of simple distillation over fractional
Easier to set up and quicker
33
Cons of simple distillation over fractional
Doesn’t separate liquids as well Should only be used if boiling temp of liquid being purified is very diff from other liquids in mixture (more than 25^C)
34
Immiscible
Doesn’t mix
35
Testing for purity
Measure boiling temp of liquid Error may be thermometer Diff organic compounds have same boiling temp
36
Homolytic fission
Breaking of a covalent bond where each of the bonding electrons leaves with one species forming a radical
37
Hydration
Adding H and OH to C=C Usually heat Allene with steam and pass mixture over catalyst of phosphoric acid.
38
Oxidation to diols
Oxidising agent = potassium manganite (VII) Acid conditions - dilute sulfuric acid Use [O] as oxidising agent
39
Heterolytic fission
Formation on ions as a result Both electrons go to one atom eg. In H-Br when bond breaks , electrons to bromine as it is more electronegative than H
40
Electrophilic addition
Electrophilic - species accepts a pair of electrons from another species and forms a covalent bond Addition - two molecules react to form a single molecule
41
Nucleophile
Species with a lone pair of electrons Forms a covalent bond with a + charges atom