Electrophilic addition reactions Flashcards

1
Q

Electrophile

A

Atom or group of atoms attracted to an electron rich centre and accepts an electron pair.

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2
Q

What type of particles are electrophiles usually?

A

Positive ions or a molecule containing a atom with a partial positive charge

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3
Q

Primary examplenof an ‘electron rich centre’

A

Double bond: Region of high e- density bc of the presence of the pi bond

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4
Q

Carbocation?

A

Molecule containing positively charge carbon atom

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5
Q

How is the major product differentiated fromt he minor

A

Major product is formed via the most stable carbocation intermediate

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6
Q

Primary carbocation

A

One alkyl group, 2 H boud to carbocation

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7
Q

Secondary carbocation

A

2 alkyl groups, 1 H bound to carbocation

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8
Q

Tertiary carbocation

A

3 alkyl groups bound to carbocation

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9
Q

In which direction does stability of carbocation intermediates increase

A

The more alkyl groups are attached to the carbocation

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10
Q

What causes the pi bond to break in the C=C during electrophilic addition and what happens immediately after

A

The e- in the pi bond are attracted to the electrophile. When the bond breaks the electrophile accepts the pair of electrons from the broken pi bond

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11
Q

How is the reaction initiated with non polar molecules

A

When the non polar molecule approaches the alkene, the e- of the pi bond induce a dipole in the previously non polar molecule.

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12
Q

What is the mechanism for reactions between alkenes and halogens/hydrogen/hydrogen halides

A

Electrophilic addition

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13
Q

How can we algerbraically represent hydrogen halides

A

HX

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