Alkenes Flashcards

1
Q

What does the double bond in alkenes cause?

A

Lack of free rotation

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2
Q

What are electrophiles?

A

Electron pair acceptors

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3
Q

What is an addition reaction?

A

An organic reaction where 2 or more molecules combine to form a larger one.

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4
Q

What are the main steps during electrophile addition reactions?

A
  1. The electrophile is attracted to the double bond
  2. They are positively charged and accept a pair of electrons from the double bond to form a single covalent bond
  3. A positive ion (carbocation) is formed
  4. A negatively charged ion forms a bond with the carbocation
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5
Q

What are the reagents and conditions in the electrophilic addition reaction with a hydrogen halide?

A
  • Reagents: Alkene and Hydrogen Halide
  • Conditions: Room temperature
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6
Q

What are the reagents and conditions and products in the electrophilic addition reaction with a halogen?

A

Reagents: Alkene and Halogen
Conditions: Room temperature
Products: Dihaloalkane

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7
Q

What are the reagents and conditions and products in the electrophilic addition with sulphuric acid to form alkyl hydrogen sulphates?

A

Reagents : Alkene and concentrated sulphuric acid
Conditions: Room temperature
Products: Alkyl hydrogen sulphates

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8
Q

What are the reagents and conditions to form an alcohol during an electrophilic addition reaction?

A

Reagents: Alkene and sulphuric acid catalyst
Conditions: Water
Product : alcohol

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9
Q

What are the reagents and conditions for the electrophilic addition reaction with phosphoric acid (H3PO4)

A

Reagents: alkene and Phosphoric acid catalyst
Conditions: Steam , 300 C and 60 atm
Product: alcohol

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10
Q

What are geometric isomers?

A

They are a form of stereo isomerism

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11
Q

What is stereoisomerism?

A
  • It is when compounds have the same structural formula but the bonds are arranged differently in space
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12
Q

State and explain the CIP rules step by step.

A
  1. Look at the carbon on the left hand side of the carbon carbon double bond and decide which has highest priority
  2. Look at the carbon on the right hand side of the carbon carbon double bond and decide which has highest priority.
  3. Look down the plane of the carbon carbon double bond and if the high priority groups are on either sides of the double bond then is it an E- isomer
    If the high priority groups are on the same side of the double bond then it is an Z-isomer
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13
Q

What are the three types of carbocation?

A

Primary , secondary and tertiary

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14
Q

What does a primary carbocation look like?

A

It has one other C attached to the C+

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15
Q

What does a secondary carbocation look like?

A

It has two other C attached to C+

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16
Q

What does a tertiary carbocation look like?

A

It has three other C attached to C+

17
Q

What is an alkyl group?

18
Q

Which type of carbocation is the most stable?

A

Tertiary carbocation

19
Q

What is the product formed from the most stable carbocation called?

A

Major product

20
Q

Why is 2-bromopropane the major product formed in the electrophilic addition of HBr?

A

Because 2-bromopropane is formed from the reaction that proceeds via the secondary carbocation which is more stable than the primary carbocation that would be formed for 1-bromopropane

21
Q

What is mechanical recycling?

A
  • It is the simplest form of recycling
  • Separates into different plastics
  • Washed, sorted and grounded up into small pellets which are melted and remoulded
22
Q

What is feedstock Recycling?

A

When polymers are heated at temperatures that break the polymer bonds and produce monomers
- It is used to make new plastics

23
Q

What are the problems with recycling?

A
  • Only done a limited number of times
  • Each heating causes some of the chains to break ( makes them shorter and degrades the properties)
24
Q

What is the definition of a polymer?

A

A long chain molecule made from lots of small molecules joined together

25
What is the definition of a monomer?
One small molecule that joins together to make polymers
26
What is addition polymerisation?
The formation of long chain molecules formed from lots of small molecules joining together with no other products
27
What must monomers have to make a polymer?
Carbon double bond
28
How can the properties of polymers be modified?
Plasticisers
29
What are plasticisers?
They are small molecules that get between the polymer chains, forcing them apart and allowing them to slide across eachother.
30
What are the conditions needed to form Low Density Poly(ethene) LDPE and what process occurs?
- High pressure (200atm) and high temperature (200 C) - O2 catalyst - Happens via free radical mechanism - Molecules loosely packed due to branching - -
31
What are the properties of Low Density Poly(ethene)?
- Flexible and soft due to molecules being loosely packed due to branching
32
What can Low Density Poly(ethene) be used for?
Bags and cling film
33
What are the conditions needed to form High Density Poly(ethene) HDPE and what process occurs?
- 60 C temperature - 2atm pressure - Ziegla-Natta catalyst
34
What are the properties of High Density Poly(ethene)
Stiff and hard due to molecules being tightly packed as there is less branching
35
What are the problems with polymers?
- Strong non-polar C-C and C-H - Very unreactive so cannot be broken down by biological agents like enzymes - Non-biodegradable - Increase in plastic litter - Animal may ingest it - Buried plastic in landfill sites which take hundreds of years to decompose