5. Alkenes Flashcards

1
Q

general formula

A

CnH2n

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2
Q

what does a C=C consist of

A

one sigma bond
one pi bond

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3
Q

Why are pi bonds vulnerable to electrophiles

A

they have a high density

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4
Q

how is a sigma bond formed in a C=C

A

one sp2 orbital from each carbon overlap to form a single C-C

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5
Q

how is pie bond formed in C=C

A
  • sideways overlap with 2 p orbitals
  • forms a pie bond above and below the plane of molecule
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6
Q

which bond is weaker: pie or sigma

A

Pie bond

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7
Q

sterioisomers

A

same structural formulae but different spatial arrangement of atoms

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8
Q

why do E-Z isomers exist

A

due to restricted rotation about the C=C

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9
Q

when do E-Z isomers arise

A
  • restricted rotation around the C=C
  • two different groups/atoms attached to the double bond
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10
Q

cis isomers

A

same side

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11
Q

Trans isomers

A

different sides

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12
Q

Alkenes with hydrogen

A
  • alkene-> alkane
  • reagent: hydrogen
  • condition: nickel catalyst
  • type of reaction: addition
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13
Q

electrophile

A

electron pair acceptor

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14
Q

reactions with halogens

A
  • reagent: bromine
  • condition: rtp
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15
Q

mechanism of reaction of alkenes with halogens + type of bond fission

A

electrophillic addition

heterolytic

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16
Q

test for alkenes

A

bromine water (orange) decolourises

17
Q

Reaction with steam

A

reagent: H2 gas
condition:
concentrated phosphoric acid
pressure (60-70)
temperature (300c)

18
Q

alkenes with potassium manganate and H+

A
  • forms diols
  • observation : KMnO4 solution turns colourless from purple
19
Q

boiling point

A

increases with molecular mass
lower than alkanes

20
Q

solubility

A

insoluble in water but soluble in organic solvents