conditions Flashcards

1
Q

To be a standard electrode potential the measurements must be made at standard conditions, namely:
3

A

1.0 mol dm-3 ions concentrations
100 kPa pressure
298 K

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2
Q

hydroenation of alkenes

A

Pt/Ni catalyst
heat

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3
Q

hydration (Steam)

A

H3PO4 catalyst (phosphoric acid)

heat

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4
Q

electrophillic sub of benzene – nitration 3

A

CONC nitric acid

CONC sulphuric acid – catalyst

60 degrees celcius

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5
Q

chlorination of benzene

A

AlCl3 – anhydrous aluminium chloride

reacts with Cl2

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6
Q

2 common reducing agents for carbonyl compounds

A

Lithium aluminium hydride, LiAlH4
- anhydrous conditions
- addition of aqueous acid
- can reduce carboxylic acids

Sodium borohydride, NaBH4
- in aqueous or alcoholic solutions
- cannot reduce carboxylic acids

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7
Q

formation of aldehyde from caboxylic acid

A

LiAlH4

refluxed in dry ether

followed by dilute acid

BUT too powerful = reduced down to alcohol so need to oxidise again

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8
Q

reduction of nirobenzene

A

reacted with tin (Sn) and CONCENTRATED HCl

heated under reflux
- boiling water bath

THEN add NaOH (second stage)

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9
Q

free radical sub / halogenation of alkanes

A

UV light – alkanes are very unreactive

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10
Q

alkene to alkane (electrophilic addition/reduction)

A

nickel catalyst

200 degrees celcius
1000 kPa

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11
Q

alkene to alcohol
hydration

A

steam + sulfuric acid

heat 300 deg c

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12
Q

halogenoalkane to alcohol (nucleophillic sub)

A

NaOH (aq)
heat under reflux

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13
Q

oxidation of alcohol

A

K2Cr2O7 (potassium dichromate VII) mixed w H2SO4
(ACIDIFIED)

heat

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14
Q

reduction of ketone / aldehyde to alcohol

A

NaBH4 (aq)

heat

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15
Q

esterification

A

alcohol + carboxylic acid

CONCENTRATED H2SO4 catalyst

heat

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16
Q

carboxylic acid to alcohol reduction

carboxylic reduction to aldehyde

A

LiAlH4 in dry ether

heat

(may be too strong, may need to oxidise alcohol to aldehyde again)

17
Q

aldehyde to carboxylic acid oxidation

A

K2Cr2O7 mixed with H2SO4
(ACIDIFIED)

heat UNDER REFLUX