alcohols and haloalkanes Flashcards

(38 cards)

1
Q

ozone initiation

A

CF2Cl2=cl. +.CFCl

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2
Q

ozone propagation

A

1) Cl.+O3=ClO+O2
2) ClO+O3=2O2+Cl.

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3
Q

ozone termination

A

1) 2O3=3O2
2) 2Cl.=Cl2

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4
Q

alcohols volatility

A

less volatile than alkanes
hydrogen bonds and vanderwaal forces

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5
Q

combustion of alcohols

A

makes co2 and water
alcohols make good fuels cus lots of energy is released

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6
Q

nucleophilic substitution reagent and condition

A

reagent aqueous NaOH
condition reflux in aqueous sol

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7
Q

nucleophile sub how does it work

A

halogens have a higher electron density than carbon and so a dipole is induced in the c-halgonen bond carbon open to attack by nucleophile

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8
Q

dehydration reaction condition

A

condition acid catalyst conc h2so4
high temp

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9
Q

oxidation of primary alcohol reagent and condition

A

reagent H2SO4/K2Cr2O7
condition distil to get aldehyde and heat under reflux to get Carboxylic Acid

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10
Q

aldehyde functional group

A

carbon double bonded oxygen and bonded hydrogen

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11
Q

ketone functional group

A

carbon double bonded to oxygen

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12
Q

esterification reagent and condition

A

reagent Carboxylic Acid + strong acid catalyst h2so4
condition

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13
Q

electrophilic addition reagent and condition

A

reagent HBr
condition room temp

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14
Q

markovnikoff rule

A

major product is formed via most stable carbocation
3>2>1

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15
Q

hydration reagent and condition

A

reagent stream (330)
condition high pressure phosphoric acid catalyst

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16
Q

phosphoric acid

17
Q

hydrogenation reagent and condition

A

reagent hydrogen
condition (finely divided) nickel catalyst

18
Q

what does free radical substitution need

19
Q

alcohols are polar because

A

large difference in electronegativity between oxygen and carbon

20
Q

polarity and solubility

A

oxygen is very electronegative so can hydrogen bond to water molecules making alcohols water soluble

21
Q

potassium dichromate color change

A

changes from orange to green when alcohol is oxidised due to change in oxidation state of chromium ion

22
Q

why cant tertiary alcohols be oxidised

A

no hydrogen attached to carbon for oxygen to remove

23
Q

hydrolysis of haloalkane forms

A

aqueous alkali

24
Q

nucleophile cub rate down group 7

A

the rate decreases
large distance between halogen nucleus and shared pair of electrons, more shielding
c-x bond enthalpy decreases
bond easier to break during rate determining step

25
electron withdrawing results in which substitution
position 3
26
electron donating results in which substitution
position 2 and 4
27
electron withdrawing groups do what
remove electron density from pi system making it less reactive
28
electron donating groups do what
donate electron density
29
NO2 donating or withdrawing
withdrawing
30
CH3 donating or withdrawing
donating
31
OH donating or withdrawing
donating
32
NH2 donating or withdrawing
donating
33
How many [H+] reducing agents needed to reduce aldehyde ketone carboxylic acid which one makes on water
2 2 4 carboxylic acid
34
Acyl chlorides can react with alcohols and phenols to form esters but requires
heat and a base and instead of making HCl makes H2O and NaCl
35
equation for making amino ethane from chloroethane
CH3CH2Cl + 2NH3 = CH3CH2NH2 + NH4Cl need hot ethanolic ammonia
36
reduction of propanenitrile equation using acid
propanentrile + HCl + 2H2O = propanoic acid + NH4Cl (ammonium chloride salt)
37
reduction of propanenitrile equation using alkali
propanentrile + NaOH+ H2O = sodium propanoate + NH3
38