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  1. Print the notecards
  2. Fold each page in half along the solid vertical line
  3. Cut out the notecards by cutting along each horizontal dotted line
  4. Optional: Glue, tape or staple the ends of each notecard together
  1. Verify Front of pages is selected for Viewing and print the front of the notecards
  2. Select Back of pages for Viewing and print the back of the notecards
    NOTE: Since the back of the pages are printed in reverse order (last page is printed first), keep the pages in the same order as they were after Step 1. Also, be sure to feed the pages in the same direction as you did in Step 1.
  3. Cut out the notecards by cutting along each horizontal and vertical dotted line
To print: Ctrl+PPrint as a list

37 notecards = 10 pages (4 cards per page)

Viewing:

crash course chem 222

front 1

Acid-Base Reaction

back 1

front 2

ELECTROPHILIC Addition to Alkenes

back 2

what is an alkene? H2C = CH2

  • a double bond between carbons

what is an electrophile?

  • an electron DEFICIENT species/molecule

front 3

NUCLEOPHILIC Addition to Alkenes

back 3

what is a nucleophile? ex) halides (I, Br, Cl)

  • an electron RICH species/molecule

front 4

Electrophilic Aromatic Substitution

back 4

front 5

Sn1, stepwise

back 5

Nucleophilic Substitution

front 6

Sn2, concerted

back 6

nucleophilic substitution

front 7

E1, stepwise

back 7

Elimination

front 8

E2, concerted

back 8

Elimination

front 9

E1cb, catalyzed by base

back 9

Elimination

front 10

Book-keeping/ Structural Reasoning

back 10

Oxidixing Reactions

  • recquires an oxidizing agent (O2, NAD)

front 11

Oxidation Mechanism

back 11

Oxidizing Reactions

  • requires an oxidizing agent (O2, NAD)

front 12

Book-keeping/Structural Reasoning

back 12

Reduction Reactions

  • requires a reducing agent (NADH)

front 13

Reduction Mechanism

back 13

Reduction Reactions

  • requires a reducing agent (NADH)

front 14

Substitution at an Acyl Group

back 14

front 15

Aldol Addition

back 15

Aldol Reactions

  • requires base

front 16

Aldol Condensation

back 16

Aldol Reactions

  • requires base

condensation = loss of H2O

front 17

Reverse Aldol Reaction

back 17

Aldol Reactions

  • requires base

front 18

back 18

Claisen Reaction

  • requires base
  • --> esters (double bond O to an R and an OR) NOT ketones (O double bond to 2 R's)

front 19

Imine Formation

back 19

Imine Creation

front 20

Transimination

back 20

Imine Creation

  • requires acid

front 21

back 21

Imine Hydrolysis

  • requires acid

front 22

back 22

Alcohol

  • Nu

front 23

back 23

Thiol

  • Nu

front 24

back 24

Amine

  • Nu

front 25

back 25

Protonated Amine

  • Nu

front 26

back 26

Carboxylic Acid

  • acyl group

front 27

back 27

Ester

  • Acyl group

front 28

back 28

Thioester

  • acyl group

front 29

back 29

Amide

  • acyl group

front 30

back 30

Carbonate

  • acyl group

front 31

back 31

Aldehyde

  • acyl group

front 32

back 32

Ketone

  • acyl group

front 33

back 33

Acyl Phosphate

  • acyl group

front 34

back 34

Imine

front 35

back 35

NADH

front 36

back 36

Benzene

front 37

back 37

NAD