ALKENES Flashcards

1
Q

What are alkenes

A

unsaturated hydrocarbons

at least one double bond

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2
Q

Why are alkenes more reactive than alkanes

A

they have double bonds which have a high electron density so can undergo addition reactions

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3
Q

What are sigma bonds

A

the overlap of 2 S orbitals, they align horizontally to form a single covalent bond

there is a strong electrostatic attraction between the nuclei and the shared pair of electrons

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4
Q

What is a pi bond

A

the parallel overlap of 2 p orbitals

when the p orbitals merge they form 2 oblong shapes, one on the top and one on the bottom

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5
Q

Why are pi bonds weaker than sigma bonds

A

the electron density is spread out above and below the nuclei, electrostatic attraction is lower as in sigma bonds the electron density is directly between the nuclei

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6
Q

What does a double bond consist of

A

a pi bond and a sigma bond

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7
Q

Stereoisomers definition

A

stereoisomers have the same structural formula but a different arrangement of atoms in space

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8
Q

When do you get E/Z isomerism

A

when you have two different atoms or groups of atoms on the same carbon in an alkene

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9
Q

Rules of naming E and Z isomers

A

Label carbons with the double 1 and 2

Find the atomic number of the element DIRECTLY BONDED TO THE C=C, the highest atomic number is given priority (if the element is the same, look further down the chain)

Use the highest priority group ON EACH CARBON to figure out if its E/Z

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10
Q

What is an electrophile and why do they attack alkenes

A

An electron pair acceptor

they are deficient in electrons so are attracted to the double bond

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11
Q

Electrophile examples

A

Positive charge ions - NO2+, H+

Polar molecules - HBr, H2SO4

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12
Q

How to convert ethene to ethane

A

Add hydrogen gas at 150 degrees with a nickel catalyst

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13
Q

Test for alkenes

A

decolouration of bromine water

from brown-orange to colourless

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14
Q

How does bromine react with alkenes

A

As Br-Br approaches the alkene it becomes polarised as electrons repelled away from the electron dense pi bond

an electron pair in the double bond is attracted to the positive dipole and forms a bond breaking the Br-Br bond

this forms a carbocation intermediate, the remaining bromine atom will have a lone pair attached which will form a bond with the positive carbon

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15
Q

How can alcohols be produced from alkenes

A

Steam and an acid catalyst

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16
Q

How to make ethanol from ethene

A

reacting with steam and phosphoric acid catalyst, 300 degrees and 60 atm of pressure

any unreacted alkene is recycled through the process

17
Q

How are halogenoalkanes formed from alkenes

A

Electrophilic addition of hydrogen halides, follows the same mechanism as halogens as Hydrogen halides are permanently polarised

18
Q

How can unsymmetrical alkenes produce multiple types of product with hydrogen halides and which type is formed more often

A

as the hydrogen can form a bond with either carbon on the double bond, leaving either a primary or secondary carbocation intermediate

the secondary carbocation intermediate will form more often as will be more stable, the halogen will then bond with this leaving the final product

19
Q

What is markownikoffs rule

A

the major product when adding a hydrogen halide to an unsymmetrical alkene is where the hydrogen adds to the carbon with the most number of hydrogens attached already

20
Q

What are the two types of polymer

A

natural - proteins and natural rubber

synthetic - poly(ethene) poly(propene)

21
Q

Properties of poly(alkenes)

A

saturated molecules

non polar

therefore unreactive

don’t degrade well in landfill