Organic chemistry Flashcards

1
Q

What is a nucleophile?

A

Negatively charged ion that donates electrons to the carbon

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2
Q

What is an electrophile?

A

Positively charged ion attracted to electrons in a double bond

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3
Q

What is heterolytic and homolytic fission?

A

Heterolytic is where the electron pair goes to one atom

X-Y —> (X+) + (Y-)

Homolytic fission is where each atom receives one electron from the bonded pair forming free radicals

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4
Q

What does free radical substitution form?

A

Turns alkanes into halgoenalkanes

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5
Q

What is reforming?

A

Turning alkanes into cycloalkanes or aromatic compounds

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6
Q

What is a sign and pi bond?

A

Sigma bond is overlap of orbitals and has high electron density so strong electrostatic attraction with the nuclei

Pi bond is weaker as overlaps sideways and has lower electron density

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7
Q

What is electrophillic addition used to make?

A

Alkene—> halogenalkane

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8
Q

How do you make an alcohol from an alkene?

A
Steam hydration (300 degrees c)
Phosphoric (v) acid catalyst
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9
Q

How do you turn a halogenalkane into an alcohol?

A

Nucleophillic substitution

(Hydrolysing)

Needs water for alkali to dissolve in and heated under reflux

Iodine hydrolysed the fastest as it has lowest bond enthalpy

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10
Q

What is nucleophillic substitution used for?

A

Turning halogenalkane into an alcohol

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11
Q

How do you turn halogenalkane into alkene?

A

Elimination reaction
Needs potassium hydroxide
Needs ethanol
Heat under reflux

R-Cl +KOH —> R + KCl + H20
(Reflux +ethanol)

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12
Q

Making chloroalkanes from alcohol

A

PCl5

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13
Q

Making bromoalkanes from alcohol

A

Needs sulphuric acid and potassium bromide

Substitution reaction

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14
Q

Make iodoalkanes from alcohol

A

Need red phosphorus

PI3

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15
Q

Alcohols can be dehydrated to form alkenes

What type of reaction and condition?

A

Elimination reaction

Acid catalyst (Conc phosphoric acid)

Heat

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16
Q

Oxidation of primary alcohols

A

With k2Cr2O7 (potassium dichromate)

Makes aldehydes then carboxylic acid

17
Q

Oxidation of secondary alcohols

A

With k2Cr2O7 (potassium dichromate)
Under reflux
Makes ketone

18
Q

Oxidation of tertiary alcohols

A

Not easily oxidised