Alkenes Ch5 Flashcards

1
Q

Bonding

Double bond formation

A

a sigma and pi bond
pi bond above and below the sigma bond

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2
Q

Shape

Shape and angle of double bond

A

Trigonal Planar + 120

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3
Q

Definition

Steroismerism

A

Molecules with some structural formula , but a different arrangement in sapce / 3D arrangement

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4
Q

Steroismerism

Geometric

A

Restricted rotation around the C=C bond
Must have 2 different atoms or groups of atoms

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5
Q

Cis/trans nameing

Cis - Alkenes

A

the Alkyl groups are on the same side (either both above or both below the double bond)

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6
Q

Cis/trans nameing

trans - alkenes

A

the alkyl groups are of opposite sides (one above, one below the double bond )

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7
Q

E/Z namig

E isomer

A

Trans- is this isomer
Use the atomic mass, the heaiver atoms on each side
opposite sides of the double bond

halogenalkenes

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8
Q

E/Z Naming

Z isomer

A

cis- is this isomer
use atomic mass to find heavier side
same side of the double bond

halogenalkenes

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9
Q

Testing for unsaturation

Bromine

Br2

A

Brown to colourless
Addition reaction

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10
Q

Testing for undsaturation

Bromine water

Br2 + H2O

A

orange to colourless
creates HBr

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11
Q

Reactions of Alkenes

Hydrogen

A

Hydrogenation reaction
NIckel Catalyst
Alkenes + H2 –> Alkane

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12
Q

Reactions of Alkenes

Halogen

A

Halogenation
Alkenes + halogen –> dihalogenalkane

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13
Q

Reactions of Alkenes

Hydrogen Halide

A

Alkenes + Hydrogen Halide –> halogenalkane

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14
Q

Reactions of Alkenes

With steam

Hot H2O (g)

A

ALlkenes + H2O (g) –> Alcohol
Phospheric acid (H3PO4) Catalyst
100% atom economy

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15
Q

Reactions of Alkenes

Oxidation to produce a diol

Contains 2 -OH groups

A

Alkene + Oxisiding agent + H2O –> Alkane diol

Potassium maganate (KMnO4)
Purple to colourless

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16
Q

Electrophilic Addition Reactions

Ethene + bromine

A

Double bond very reactive
Hetrolytic Fission
Carbocatio is formed
Br+ is the electrophile

17
Q

Electrophilic Addition Reactions

With HBr

A

Ethene symmetrical reacts to form bromoethane an asymmetrical

18
Q

Electrophilic Addition Reactions

Propene + hydrogen Bromide

A

Both molecules are asymmetrical
2-bromopropane major product
-seconday carbocation formed in the mechanism when H bonds to the Carbon 1 is more stable than if a primary carbocation was formed

19
Q

Definition

Addition Polymerisation

A

The joining together of many small monomers to produce a long chain through the breaking of a C=C double bond

20
Q

Polymer waste

A
  1. Land fill (they don’t decompose)
  2. Recycling (sorted by type and remoulded)
  3. Combustion (Provides energy / gases could be toxic )
21
Q

Biodegradeable polymers

uses, disadvantages and source

A

Corn or starch
uses : compostable cups and cutley
Disadvantages: Needs lots of land
C & H produced on teh reak down cannot be used directly