RPA Flashcards

1
Q

HNO3 and H2SO4 as catalyst in nitrification of benzene

A

HNO3 + 2H2SO4 -> NO2^+ + 2HSO4^- + H3O^+

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2
Q

Test for aldehyde

A

Tollens’ = silver mirror

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3
Q

Test for carboxylic acid

A

Carbonate = effervescence

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4
Q

Retention time

A

The time taken from injection of the sample for the component to leave the column

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5
Q

Reasons to not have stereoisomers

A
  • production of single isomer more expensive

- one of the isomers may be toxic

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6
Q

Alpha amino acid

A

Both NH2 and COOH are joined to the same C

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7
Q

Evidence against Kekule’s structure of benzene:

A
  • Bond length different from short C=C, long C-C
  • enthalpy change if hydrogenation less ectothermic than expected
  • only reacts with Br2 at high temperatures and with a halogen carrier
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8
Q

Why Cr2O7^2- over MnO4^-?

A

Ecell for MnO4^- is more positive than “species A”

MnO4^- reacts with “species A”

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9
Q

Under what circumstances can an optical isomer form?

A

If a chiral carbon is present

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10
Q

What are the chemicals needed to nitrate a benzene ring?

A

HNO3 and H2SO4

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11
Q

What are the reagents needed to halogenated a benzene ring?

A

FeCl3 or AlCl3

And Cl2

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12
Q

What are the reagents needed to animate a nitro group on a benzene ring?

A

Sn and HCl

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13
Q

Tests for ketones?

How to test which ketone if multiple could be chemical?

A

2,4-DNPH, orange ppt
Tollens’ reagent, no reaction

Purify 2,4-DNPH derivative and measure melting point. Compare to database

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14
Q

H H O
OH—C—C—-C—OH
H H

Eliminate H2O

A

H OH
C==C
H COOH

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15
Q

H OH
C==C
H COOH

Reduce

A

H. H
C==C
H CH2OH

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16
Q

Reduction of a carboxylic acid gives…

A

An alcohol

17
Q

And oxidation of an alcohol gives…

A

Aldehyde then carboxylic acid

18
Q

How does a liquid stationary phase separate the organic compound in a mixture

A

Relative solubility