Reagents With Organic Chem Flashcards

1
Q

Elimination of an alcohol gives what product, using what reagent

A

Reagent =Concentrated acid e.g. H2SO4, H+

Product = alkene

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2
Q

Hydration of an alkene forms
what product,
using what reagent

A

Product=alcohol

Reagent= dilute acid (H2SO4 + H2O ; H3O+)

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3
Q

How do we ensure halohydrin formation instead of dihalogenation?
Which 2 reagents allows this?

A

NBS (N-Bromo succinimide) and water

Same time

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4
Q

What 4 metal catalysts do we use in hydrogenation and they are often with carbon

A

Pd, Pt, Ni, Fe

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5
Q

Which catalyst with H2 on reacts with alkynes .

It is therefore called……

A

Lindlar

Chemoselective

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6
Q

Sn1 reaction only work with what alcohols

A

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7
Q

What 2 reagents dont go through carbocation to form halogenoalkanes from alcohols

A
  1. SOCl2 (thionyl chloride)

2. PBr3 (phosphorus tribromide)

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8
Q

What are 2 ways to make carbonyl compounds

A
  1. Oxidation of 1° and 2° alcohols

2. From ozonolysis of alkenes

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9
Q

What reagent can be used by both

1° alcohol to form an aldehyde

and
2° alcohols to form a ketone

A

PCC , THF (together)

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10
Q

What reagent can only be used by 2° alcohols to form an aldehyde

A

Jones reagent with water

CrO3, H2SO4 and H2O same time

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11
Q

If you added Jones reagent to a 1° alcohol what would you get instead of a carbonyl

A

A carboxylic acid

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12
Q

What are the 5 reactions of aldehydes and ketones and their products

A
  1. Grignard reactions = alcohol
  2. Acetal formation = acetal
  3. Imine formation= imine
  4. Reduction = alcohol
  5. Cyanohydrin formation= cyanohydrin formation
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13
Q

What do you have to add to a halogenoalkane to form a grignard reagent

A

Mg and THF

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14
Q

What do you have to add to a carbonyl group to get an imine (2)

A

1° anine and H3O+ at same time

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15
Q

What are our 2 reducing agents for carbonyl compounds to form alcohols

A
  1. LiAlH4 (LAH) lithium diminium hydride

2. NaBH4 sodium borohydride

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16
Q

What 2 reagents do we need to get a cyanohydrin from a carboxylic acid

A

NaCN and HCN together st same time

17
Q

What 2 reagents do we have to add to a carbonyl group to get an acetal

A

ROH and H3O+

18
Q

What are the 3 ways of making carboxylic acids

A
  1. Oxidation of a 1° alcohol using Jones reagent CrO3, H2SO4 with H2O
  2. Grignard reagent + CO2
  3. Hydrolysis of carboxylic acid derivatives using either
    - H2SO4, H2O
    Or
    -NaOH, H20
19
Q

What are th 5 derivatives of carboxylic acids

A
  1. Acid or Acyl chloride
  2. Acid anhydride
  3. Nitrile
  4. Amide
  5. Ester
20
Q

What are 2 ways to synthesize esters using carboxylic acids

A
  1. Fischer esterification (add an alcohol)

2. SN2 reaction with an alkyl halide (halogenoalkane )