Alkenes Flashcards

1
Q

What is an electrophile?

A

Attracted to a negativity, and electron pair accepter

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2
Q

How many products are formed in an electophilic addition reaction?

A

1

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3
Q

Where are electrophiles attracted to on alkenes?

A

The carbon to carbon double bond, which is electron dense

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4
Q

What are 3 examples of electrophiles?

A
  • Br2
  • HBr
  • H2SO4
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5
Q

What is the first thing that happens in electrophilic addition (between Br2 and ethene)?

A

A dipole is induced in Br2, which is caused by repulsion from the electron dense double bond in ethene

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6
Q

Draw the reaction mechanism when an alkene reacts with HBr, include intermediate steps

A

http://alevelchem.com/img/electrophilic_addition_hydrogen_bromide.gif

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7
Q

What is a common reaction in alkenes? Why?

A

Electrophilic addition
As the C=C bond creates and electron dense area that attracts electrophiles

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8
Q

What are the 4 steps of electrophilic addition reactions?

A

1) electrophile is attracted to the double bond
2) Electrophiles accept a pair of electrons from the double bond
3) A carbocation is formed
4) a negatively charged ion forms a bond with the carbocation

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9
Q

Why don’t pi bonds rotate?

A

Any rotation would break the pi bond, because the p orbitals above and below would no longer overlap

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10
Q

Why are products in electrophilic substitution formed in different amounts?

A
  • The major product is formed via a tertiary carbocation intermediate and the minor product is formed via a secondary carbocation intermediate
  • The tertiary carbocation is more stable than the secondary/primary carbocation
  • because it has a greater positive inductive effect
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11
Q

What classification is the most stable carbocation?

A

tertiary (primary is the least)

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12
Q

In addition polymerisation, what will high temperatures and pressures cause?

A

branched chain polymers with weak intermolecular forces

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13
Q

What is the positive inductive effect?

A

more carbon atoms cause e- density to be shifted towards the carbocation, making it more stable

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14
Q

Why is a tertiary carbocation more stable than a secondary carbocation?

A

As it has a greater positive inductive effect

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15
Q

What 2 step reaction can form alcohols from alkenes?

A

1) reaction with cold, conc. H2SO4
2) reaction with cold water

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16
Q

Name the mechanism for the reaction of concentrated H2SO4 with an alkene…

A

electrophilic addition

17
Q

Why does E-Z isomerism occur in alkenes?

A

C=C bonds cannot rotate