• Shuffle
    Toggle On
    Toggle Off
  • Alphabetize
    Toggle On
    Toggle Off
  • Front First
    Toggle On
    Toggle Off
  • Both Sides
    Toggle On
    Toggle Off
  • Read
    Toggle On
    Toggle Off
Reading...
Front

Card Range To Study

through

image

Play button

image

Play button

image

Progress

1/30

Click to flip

Use LEFT and RIGHT arrow keys to navigate between flashcards;

Use UP and DOWN arrow keys to flip the card;

H to show hint;

A reads text to speech;

30 Cards in this Set

  • Front
  • Back

Alkene to Alkane

•add H2 with a nickel catalyst

Alkene to haloalkane

•add HCl


•electrophilic addition

How do you make an ester?

alcohol + carboxylic acid with H2SO4 and heat

Nitrobenzene to ...


(NO2 to NH2)

tin metal, concentrated HCl and Reflux

How many [H] are added and how many H2O are made?

•6[H]


•2H2O

Alcohol to alkene

•dehydration


H3PO4

Alcohol to alkene

•dehydration


steam


H3PO4


•heat - 300 degrees


65 atm

Alcohol to haloalkane (bromoalkane)

NaBr and H2SO4

What catalyst is used in a reaction of ketones are aldehydes to make an alcohol ?

•reduction - NaBH4

Oxidation of a primary alcohol


•reflux product


•distil product


•amount of [O] added


•water produced ? How many ?

•reflux - carboxylic acid, 1H20, 2[O]


•distil aldehyde, 1H2O, 1[O]

Oxidation of a primary alcohol


•reflux product


•distil product


•amount of [O] added


•water produced ? How many ?

•reflux - carboxylic acid, 1H20, 2[O]


•distil aldehyde, 1H2O, 1[O]

Oxidation of secondary alcohol?


•catalyst?


•product ?


•reflux or distil ?


•how much water is produced


•how many [O] used ?

K2Cr2O7 / H2SO4


•ketone


•reflux


•1H2O


•1[O]

Oxidation of a primary alcohol


•reflux product


•distil product


•amount of [O] added


•water produced ? How many ?

•reflux - carboxylic acid, 1H20, 2[O]


•distil aldehyde, 1H2O, 1[O]

Oxidation of secondary alcohol?


•catalyst?


•product ?


•reflux or distil ?


•how much water is produced


•how many [O] used ?

K2Cr2O7 / H2SO4


•ketone


•reflux


•1H2O


•1[O]

Aldehyde to a carboxylic acid?

K2Cr2O7


•reflux


•1[O]


•no water

Bromination of benzene

Br2 and AlBr3


•electrophilic substitution

Bromination of benzene

Br2 and AlBr3


•electrophilic substitution

Adding CN (increasing the carbon chain)

NaCN and H2SO4

Bromination of benzene

Br2 and AlBr3


•electrophilic substitution

Adding CN (increasing the carbon chain)

NaCN and H2SO4

Hydroxynitrile to a carboxylic acid

H2O and HCl

Bromination of benzene

Br2 and AlBr3


•electrophilic substitution

Adding CN (increasing the carbon chain)

NaCN and H2SO4

Hydroxynitrile to a carboxylic acid

H2O and HCl

Hydroxynitrile to an anime

H2 and a Nickel catalyst

Amine to an ammonium salt

excess HCl

Aldehyde to hydroxynitrile

HCN


•nucleophilic addition

Haloalkane to an amine

excess NH3


Ethanol

Acylation of benzene

•acyl chlorine


AlCl3

Carboxylic acid group on a phenol to a salt

Na2CO3


Or


NaOH to add salt group on carboxylic acid and phenol (OH)