-oicacidsuffixforCOOHsilvermirrorformationpositiveTollen'stestaldaricacidstrongoxidation ofsugarproduces an:decarboxylationremovesa CO2from themoleculeCOOHabbreviationfor acarboxylicacidketoacidpolyfunctionalacid withcarbonylgroupalwaysfound at endof parentchainCOOHand CHOgroupsare:aldonicacidweakoxidation ofsugarproduces an:hemiacetalcontains -OH and -ORon samecarbonenantiomersnon-superimposablemirror imageshydroxyacidspolyfunctionalacid withhydroxylgroupsucrosedisaccharidewith glucose+ fructoseacidicpolysaccharideheparinandhyaluronicacid are:acetaldehydealdehydecommonname w/ 2carbonsreducingsugarsugar withfreeanomericcarbon(sucrose)lactosedisaccharidewith 2glucose +galactosecarboxylateionproductwhen COOHreacts w/waterD-enantiomerbiologicallyrelevantcarbohydratesamylopectinpolysaccharidewith all glucose,alpha 1-4bonds, andsome alpha 1-6branch pointsformaldehydealdehydecommonname w/ 1carbonsacetalcontains 2 -OR groupson samecarbonmilksugarlactoseis knownas a:L-enantiomerhas -OHon left sideof Fisherprojectionsecondaryalcoholproductwhenketone isreducedamylosepolysaccharidewith all glucose,alpha 1-4bonds, and nobranch pointsvalericacidcommonname forCOOH w/5 carbonscellobiosedisaccharidewith 2glucosesand beta1-4linkageketopentosecarb withketoneand 5carbonscarboxylicacidderivativesacidchloride,acidanhydride,and amide-oatesuffix foracylportion ofan esterbetaanomeranomericcarbonpointsdownmaltosedisaccharidewith 2glucosesand alpha 1-4 linkageCH2OHpointsdownhow to IDthe L-enantiomerfor cycliccarbsbutyraldehydealdehydecommonname w/ 4carbonsbrainsugargalactoseis knownas a:aldehydeproductwhen oxidizea primaryalcoholformicacidcommonname forCOOH w/1 carboncellulosepolysaccharidewith all glucose,beta 1-4 bonds,and no branchpointsstructuralpolysaccharidescelluloseand chitinare:saponificationhydrolysisof esterunder basicconditionsunsaturatedacidpolyfunctionalacid withdouble bondsCH2OHpointsuphow to IDthe D-enantiomerfor cycliccarbsdiastereomersisomersthat arenot mirrorimagespropionaldehydealdehydecommonname w/ 3carbons-onesuffixused fornamingketonescarboxylicacidproductwhenoxidize analdehydealdohexosecarb withaldehydeand 6carbonsalditolreductionof sugarproducesan:alphaanomeranomericcarbonpointsdowncarbonylcompoundshave anon-polarC-Z bondcarboxylicacid saltproductwhen COOHreacts w/ astrong basestoragepolysaccharidesstarchandglycogenare:esterproductwhen COOHreacts w/ analcoholtest foraldehydesBenedict'sTestchiralcarbon w/4 differentgroupsacylcompoundshave apolar C-Z bond-alsuffixused fornamingaldehydesaceticacidcommonname forCOOH w/2 carbons-oicacidsuffixforCOOHsilvermirrorformationpositiveTollen'stestaldaricacidstrongoxidation ofsugarproduces an:decarboxylationremovesa CO2from themoleculeCOOHabbreviationfor acarboxylicacidketoacidpolyfunctionalacid withcarbonylgroupalwaysfound at endof parentchainCOOHand CHOgroupsare:aldonicacidweakoxidation ofsugarproduces an:hemiacetalcontains -OH and -ORon samecarbonenantiomersnon-superimposablemirror imageshydroxyacidspolyfunctionalacid withhydroxylgroupsucrosedisaccharidewith glucose+ fructoseacidicpolysaccharideheparinandhyaluronicacid are:acetaldehydealdehydecommonname w/ 2carbonsreducingsugarsugar withfreeanomericcarbon(sucrose)lactosedisaccharidewith 2glucose +galactosecarboxylateionproductwhen COOHreacts w/waterD-enantiomerbiologicallyrelevantcarbohydratesamylopectinpolysaccharidewith all glucose,alpha 1-4bonds, andsome alpha 1-6branch pointsformaldehydealdehydecommonname w/ 1carbonsacetalcontains 2 -OR groupson samecarbonmilksugarlactoseis knownas a:L-enantiomerhas -OHon left sideof Fisherprojectionsecondaryalcoholproductwhenketone isreducedamylosepolysaccharidewith all glucose,alpha 1-4bonds, and nobranch pointsvalericacidcommonname forCOOH w/5 carbonscellobiosedisaccharidewith 2glucosesand beta1-4linkageketopentosecarb withketoneand 5carbonscarboxylicacidderivativesacidchloride,acidanhydride,and amide-oatesuffix foracylportion ofan esterbetaanomeranomericcarbonpointsdownmaltosedisaccharidewith 2glucosesand alpha 1-4 linkageCH2OHpointsdownhow to IDthe L-enantiomerfor cycliccarbsbutyraldehydealdehydecommonname w/ 4carbonsbrainsugargalactoseis knownas a:aldehydeproductwhen oxidizea primaryalcoholformicacidcommonname forCOOH w/1 carboncellulosepolysaccharidewith all glucose,beta 1-4 bonds,and no branchpointsstructuralpolysaccharidescelluloseand chitinare:saponificationhydrolysisof esterunder basicconditionsunsaturatedacidpolyfunctionalacid withdouble bondsCH2OHpointsuphow to IDthe D-enantiomerfor cycliccarbsdiastereomersisomersthat arenot mirrorimagespropionaldehydealdehydecommonname w/ 3carbons-onesuffixused fornamingketonescarboxylicacidproductwhenoxidize analdehydealdohexosecarb withaldehydeand 6carbonsalditolreductionof sugarproducesan:alphaanomeranomericcarbonpointsdowncarbonylcompoundshave anon-polarC-Z bondcarboxylicacid saltproductwhen COOHreacts w/ astrong basestoragepolysaccharidesstarchandglycogenare:esterproductwhen COOHreacts w/ analcoholtest foraldehydesBenedict'sTestchiralcarbon w/4 differentgroupsacylcompoundshave apolar C-Z bond-alsuffixused fornamingaldehydesaceticacidcommonname forCOOH w/2 carbons

CH 107 Exam 2 Review - Call List

(Print) Use this randomly generated list as your call list when playing the game. There is no need to say the BINGO column name. Place some kind of mark (like an X, a checkmark, a dot, tally mark, etc) on each cell as you announce it, to keep track. You can also cut out each item, place them in a bag and pull words from the bag.


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  1. suffix for COOH
    -oic acid
  2. positive Tollen's test
    silver mirror formation
  3. strong oxidation of sugar produces an:
    aldaric acid
  4. removes a CO2 from the molecule
    decarboxylation
  5. abbreviation for a carboxylic acid
    COOH
  6. polyfunctional acid with carbonyl group
    keto acid
  7. COOH and CHO groups are:
    always found at end of parent chain
  8. weak oxidation of sugar produces an:
    aldonic acid
  9. contains -OH and -OR on same carbon
    hemiacetal
  10. non-superimposable mirror images
    enantiomers
  11. polyfunctional acid with hydroxyl group
    hydroxy acids
  12. disaccharide with glucose + fructose
    sucrose
  13. heparin and hyaluronic acid are:
    acidic polysaccharide
  14. aldehyde common name w/ 2 carbons
    acetaldehyde
  15. sugar with free anomeric carbon (sucrose)
    reducing sugar
  16. disaccharide with 2 glucose + galactose
    lactose
  17. product when COOH reacts w/ water
    carboxylate ion
  18. biologically relevant carbohydrates
    D-enantiomer
  19. polysaccharide with all glucose, alpha 1-4 bonds, and some alpha 1-6 branch points
    amylopectin
  20. aldehyde common name w/ 1 carbons
    formaldehyde
  21. contains 2 -OR groups on same carbon
    acetal
  22. lactose is known as a:
    milk sugar
  23. has -OH on left side of Fisher projection
    L-enantiomer
  24. product when ketone is reduced
    secondary alcohol
  25. polysaccharide with all glucose, alpha 1-4 bonds, and no branch points
    amylose
  26. common name for COOH w/ 5 carbons
    valeric acid
  27. disaccharide with 2 glucoses and beta1-4 linkage
    cellobiose
  28. carb with ketone and 5 carbons
    ketopentose
  29. acid chloride, acid anhydride, and amide
    carboxylic acid derivatives
  30. suffix for acyl portion of an ester
    -oate
  31. anomeric carbon points down
    beta anomer
  32. disaccharide with 2 glucoses and alpha 1-4 linkage
    maltose
  33. how to ID the L-enantiomer for cyclic carbs
    CH2OH points down
  34. aldehyde common name w/ 4 carbons
    butyraldehyde
  35. galactose is known as a:
    brain sugar
  36. product when oxidize a primary alcohol
    aldehyde
  37. common name for COOH w/ 1 carbon
    formic acid
  38. polysaccharide with all glucose, beta 1-4 bonds, and no branch points
    cellulose
  39. cellulose and chitin are:
    structural polysaccharides
  40. hydrolysis of ester under basic conditions
    saponification
  41. polyfunctional acid with double bonds
    unsaturated acid
  42. how to ID the D-enantiomer for cyclic carbs
    CH2OH points up
  43. isomers that are not mirror images
    diastereomers
  44. aldehyde common name w/ 3 carbons
    propionaldehyde
  45. suffix used for naming ketones
    -one
  46. product when oxidize an aldehyde
    carboxylic acid
  47. carb with aldehyde and 6 carbons
    aldohexose
  48. reduction of sugar produces an:
    alditol
  49. anomeric carbon points down
    alpha anomer
  50. have a non-polar C-Z bond
    carbonyl compounds
  51. product when COOH reacts w/ a strong base
    carboxylic acid salt
  52. starch and glycogen are:
    storage polysaccharides
  53. product when COOH reacts w/ an alcohol
    ester
  54. Benedict's Test
    test for aldehydes
  55. carbon w/ 4 different groups
    chiral
  56. have a polar C-Z bond
    acyl compounds
  57. suffix used for naming aldehydes
    -al
  58. common name for COOH w/ 2 carbons
    acetic acid