Electrophilic addition in alkenes Flashcards

1
Q

What is an electrophile?

A
  • Electrophile is an electron pair acceptor and is attracted to an electron-rich centre.
  • Positively charged ions are electrophiles.
  • Polar molecules can also be electrophiles as the partially positive atom is attracted to places with electrons.
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2
Q

Electrophilic addition

A
  • The double bond in an alkene represents a region of high electron density because of the presence of pi-electrons.
  • This high electron density of pi-electrons attracts electrophiles.
  • The double bond in alkene opens up and atoms are added to the carbon atoms.
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3
Q

Mechanism of electrophilic addition of polar molecule

A
  • 2 electrons from the C=C attack the partially positive X atom, creating new bond between Carbon 1 and X atom.
  • X-Y bond breaks by HETEROLYTIC fission.
  • Electrons are taken by Y atom to form a negative ion w/ lone pair.
  • Carbon 2 is electron deficient as C1 took the electrons to form bond w/ X atom when double bond broke.
  • So C2 is a positively charged CARBOCATION.
  • Y atom acts as a NUCLEOPHILE, donates its lone pair and forms bond w/ C2.
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4
Q

What is a nucleophile and carbocation?

A
  • Nucleophile is an electron pair donor.

- Carbocation is an organic ion containing a positively charged carbon atom.

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5
Q

Mechanism for electrophilic addition of non-polar halogens

A
  • When halogen approaches an alkene, the double bond repels the electrons in halogen molecule, polarising Hal-Hal. This is an INDUCED DIPOLE.
  • HETEROLYTIC fission of halogen molecule. The partially pos. halogen bonds to C1.
  • Positively charged carbocation attracts the negative halogen.
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6
Q

Markownikoff’s rule

A
  • If hydrogen halide adds to symmetrical alkene like ethene, only 1 possible product. If it adds to an unsym. alkene, 2 possible products w/ halogen on either carbons.
  • Markownikoff’s rule says that the major product from addition of a hydrogen halide to an unsymmetrical alkene, is the one where hydrogen adds to the carbon w/ the most hydrogens already attached.
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7
Q

Carbocation stability

A
  • Amount of each product formed depends on how stable the carbocation formed is.
  • 3 possible carbocations: primary (2H 1 Alkyl), secondary (1H 2 Alkyl) and tertiary (0H 3 Alkyl).
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