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Last updated 8:25 AM on 2/4/26
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18 Terms

1
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Why does 4-nitrophenol have a higher boiling point than 2-nitrophenol?

2
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Compare the bromination of benzene vs. phenol (conditions and reasoning).

  • both undergo electrophilic attack

  • bromination of phenol is tribromination and bromination of benzene monobromination

  • bromination of benzene requires a halogen carrier such as AlBr3 but phenol does not

3
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How does the O−H absorption differ between ethanoic acid and ethanol in an IR spectrum?

ethanoic acid - very broad peak at 2500-3300

ethanol - broad smooth 3230-3550

key distinction is that ethanoic acid has a peak at 1700 due to presence of c=o

4
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How does the OH bond in a carboxylic acid differ from the OH bond in an alcohol in terms of infrared spectroscopy

The OH bond in a carboxylic acid shows a distinct, extremely broad absorption in IR spectroscopy, generally occurring between

2500--3300cm-1

(often overlapping with C-H stretches), whereas an alcohol's OH bond appears as a strong, broad peak at a higher wavenumber, typically

3200-3600

5
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What are the two-stage observations when adding butylamine dropwise, then in excess, to aqueous copper(II) sulfate?

  • at first a light blue precipitate is formed

  • when excess the precipitate redissolves to form a deep blue solution

6
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Write the equation for the reaction of [Cu(H2​O)6​]2+ with dropwise butylamine (RNH2​). What is the role of the amine here?

[Cu(H20)6}2+ + 2CH3CH2CH2CH2NH2 —> [Cu(H20)4(OH)2 + 2CH3CH2CH2CH2NH3+

  • amine acts as a base (accepts proton from water ligand)

7
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Write the equation for the excess addition of butylamine (RNH2​) to the copper(II) hydroxide precipitate. What is the role of the amine here?

[Cu(H20)6]2+ + 4CH3CH2CH2CH2NH2 —→ [Cu(CH3CH2CH2CH2NH2)4(H20)2] 2+ + 2OH- + 2H20

  • the amine acts as a ligand

8
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explain why different alkanes in crude oil can be separated by fractional distillation?

Different alkanes have different boiling points based on their carbon chain length and molar mass

9
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Why does the reactivity of primary halogenoalkanes increase from chloro- to iodoalkanes? (3 Marks)

  • down the group the halogen atom gets larger

  • distance between 2 nuclei increases so the C-X bond length increases

  • the C-X bond becomes weaker and requires less energy to overcome

10
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"Compare the rates of hydrolysis of 1-chlorobutane and 2-chloro-2-methylpropane."

  • 1-chlorobutane is primary; 2-chloro-2-methylpropane is tertiary.

  • Tertiary halogenoalkanes react via SN​1, while primary react via SN​2.

  • The SN​1 mechanism is faster because it involves the formation of a stable tertiary carbocation.

  • Inductive Effect: Mention that the three alkyl groups "push" electron density toward the positive carbon, stabilizing it (the inductive effect).

11
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difference in drawing out the mechanism for a primary and tertiary halogenoalkane?

SN1 VS SN2

sn2 - contains a transition state

sn1 - draw two steps (halogen leaving - carbocation intermediate)

12
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How does the classification (type) of a halogenoalkane affect its rate of reaction?

Tertiary > Secondary > Primary

  • Tertiary halogenoalkanes react via the SN​1 mechanism.

  • Stability: This mechanism involves a carbocation intermediate.

  • Inductive Effect: Tertiary carbocations are the most stable because they have three alkyl groups that donate electron density (positive inductive effect) to reduce the charge density on the carbon atom.

13
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Describe the stages by which a catalytic converter converts polluting gases in a car exhaust system? (3 marks)

  • adsorption of gases to catalytic surface

  • weakening of bonds on catalytic surface

  • desorption of products from catalytic surface

14
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What are the conditions and reactants required for the conversion of benzene to nitrobenzene?

conc. HNO3 and H2SO4 heated under reflux with 50 degrees

15
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COnditions and reactant required for the conversion of nitrobenzene to a phenyl amine

conc HCl and Tin - heated under reflux

16
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What two reactions can be done to nitriles?

hydrolysed and reduction

17
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Conditions and reactant required for the hydrolysis of a nitrile

acidic hydrolysis : dilute HCl heated under reflux to form carboxylic acid and ammonium salt

alkaline hydrolysis : NaOH and h20 heated under reflux to form sodium carboxylate salt and ammonia gas

18
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Write a full redox equation from the half equations for following the two changes combined

MnO4- —> Mn2+

C2O4 2- —> CO2

2MnO4_ + 16H+ + 5C204 2- —> 2Mn2+ + 8H20 + 10CO2

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