Alkenes Flashcards

1
Q

What is the bond angle around the C=C bond?

A

120

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2
Q

How is a pi bond formed?

A

•by the sideways overlap of two p oribtals on each carbon atom forming a pi bond above and below the plane of molecule

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3
Q

What is a addition reaction?

A

Where two molecules react to produce one

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4
Q

Reaction of alkenes with hydrogen?

A
  • hydrogen adds across the double bond to form a saturated alkane
  • nickel catalyst
  • e.g ethene + H2 –> ethane
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5
Q

Why do addition reactions happen?

A

• the double bond has plenty of electrons and is easily attacked by electrophiles

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6
Q

How does the double bond behave like a nucleophile ?

A

• its attracted to places with not a lot of electrons

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7
Q

How is magarine manufactured?

A

• by the hydrogenation of vegetable oil

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8
Q

How do you test for the presence of a double bond?

A

• when an alkene e.g cyclohexane is bubbled through an orange solution of bromine at room temp the solution goes from Orange –> colourless

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9
Q

What do reactions with hydrogen halides form?

A

• halogenalkanes

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10
Q

When non symmetrical molecules and hydrogen halides react with alkenes, why do some give rise to two products?

A

• because the alkenes unsymmetrical

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11
Q

Reaction with steam?

A
  • steam can be added across double bond to form alcohols
  • pressure : 60atm
  • catalyst : phosphoric acid
  • temperature : 600K
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12
Q

Why do reaction with steam have a high atom economy?

A

• because there are no ware products

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13
Q

Why are alkenes more reactive than alkanes?

A

• because they contain a high electron density in the double bond

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14
Q

Explanation of electrophillic addition

e.g C2H4 + Br2 –> C2H4Br2

A
  • as the bromine molecule approaches the ethene is becomes polarised by the high density of electrons present in the double bond. The pi bond breaks and an electron pair forms a new bond with the + charged bromine atom
  • at the same time that the bond is formed between the carbon and bromine the Br-Br bond breaks (hetrolytic fission) to form a bromide ion and carbon cation
  • carboncations are highly reactive and the bromide reacts rapidly with it. A covalent bond is formed between the carboncation and bromide ion
  • in the mechanism, the polarised bromine molecule has behaved like an electrophile. The bromine is attracted to the double bond where it accepts a pair of electrons to form a new covalent bond
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