saponificationhydrolysisof esterunder basicconditionsketopentosecarb withketoneand 5carbonsaldonicacidweakoxidation ofsugarproduces an:diastereomersisomersthat arenot mirrorimagesaceticacidcommonname forCOOH w/2 carbonsCOOHabbreviationfor acarboxylicacidstoragepolysaccharidesstarchandglycogenare:amylosepolysaccharidewith all glucose,alpha 1-4bonds, and nobranch pointsunsaturatedacidpolyfunctionalacid withdouble bondstest foraldehydesBenedict'sTestformicacidcommonname forCOOH w/1 carboncarboxylicacidproductwhenoxidize analdehydehydroxyacidspolyfunctionalacid withhydroxylgroupesterproductwhen COOHreacts w/ analcoholmilksugarlactoseis knownas a:acylcompoundshave apolar C-Z bondacetaldehydealdehydecommonname w/ 2carbonsaldaricacidstrongoxidation ofsugarproduces an:amylopectinpolysaccharidewith all glucose,alpha 1-4bonds, andsome alpha 1-6branch pointsalditolreductionof sugarproducesan:carboxylateionproductwhen COOHreacts w/wateraldohexosecarb withaldehydeand 6carbonschiralcarbon w/4 differentgroupsD-enantiomerbiologicallyrelevantcarbohydratesalwaysfound at endof parentchainCOOHand CHOgroupsare:butyraldehydealdehydecommonname w/ 4carbonsstructuralpolysaccharidescelluloseand chitinare:betaanomeranomericcarbonpointsdownCH2OHpointsuphow to IDthe D-enantiomerfor cycliccarbsaldehydeproductwhen oxidizea primaryalcohol-alsuffixused fornamingaldehydesenantiomersnon-superimposablemirror imagesmaltosedisaccharidewith 2glucosesand alpha 1-4 linkagevalericacidcommonname forCOOH w/5 carbonssecondaryalcoholproductwhenketone isreducedformaldehydealdehydecommonname w/ 1carbonscellulosepolysaccharidewith all glucose,beta 1-4 bonds,and no branchpointscarboxylicacidderivativesacidchloride,acidanhydride,and amidelactosedisaccharidewith 2glucose +galactosebrainsugargalactoseis knownas a:acidicpolysaccharideheparinandhyaluronicacid are:reducingsugarsugar withfreeanomericcarbon(sucrose)decarboxylationremovesa CO2from themoleculesucrosedisaccharidewith glucose+ fructosesilvermirrorformationpositiveTollen'stestpropionaldehydealdehydecommonname w/ 3carbons-onesuffixused fornamingketonesacetalcontains 2 -OR groupson samecarbon-oatesuffix foracylportion ofan esterL-enantiomerhas -OHon left sideof FisherprojectionCH2OHpointsdownhow to IDthe L-enantiomerfor cycliccarbsketoacidpolyfunctionalacid withcarbonylgroupalphaanomeranomericcarbonpointsdowncellobiosedisaccharidewith 2glucosesand beta1-4linkagehemiacetalcontains -OH and -ORon samecarbon-oicacidsuffixforCOOHcarboxylicacid saltproductwhen COOHreacts w/ astrong basecarbonylcompoundshave anon-polarC-Z bondsaponificationhydrolysisof esterunder basicconditionsketopentosecarb withketoneand 5carbonsaldonicacidweakoxidation ofsugarproduces an:diastereomersisomersthat arenot mirrorimagesaceticacidcommonname forCOOH w/2 carbonsCOOHabbreviationfor acarboxylicacidstoragepolysaccharidesstarchandglycogenare:amylosepolysaccharidewith all glucose,alpha 1-4bonds, and nobranch pointsunsaturatedacidpolyfunctionalacid withdouble bondstest foraldehydesBenedict'sTestformicacidcommonname forCOOH w/1 carboncarboxylicacidproductwhenoxidize analdehydehydroxyacidspolyfunctionalacid withhydroxylgroupesterproductwhen COOHreacts w/ analcoholmilksugarlactoseis knownas a:acylcompoundshave apolar C-Z bondacetaldehydealdehydecommonname w/ 2carbonsaldaricacidstrongoxidation ofsugarproduces an:amylopectinpolysaccharidewith all glucose,alpha 1-4bonds, andsome alpha 1-6branch pointsalditolreductionof sugarproducesan:carboxylateionproductwhen COOHreacts w/wateraldohexosecarb withaldehydeand 6carbonschiralcarbon w/4 differentgroupsD-enantiomerbiologicallyrelevantcarbohydratesalwaysfound at endof parentchainCOOHand CHOgroupsare:butyraldehydealdehydecommonname w/ 4carbonsstructuralpolysaccharidescelluloseand chitinare:betaanomeranomericcarbonpointsdownCH2OHpointsuphow to IDthe D-enantiomerfor cycliccarbsaldehydeproductwhen oxidizea primaryalcohol-alsuffixused fornamingaldehydesenantiomersnon-superimposablemirror imagesmaltosedisaccharidewith 2glucosesand alpha 1-4 linkagevalericacidcommonname forCOOH w/5 carbonssecondaryalcoholproductwhenketone isreducedformaldehydealdehydecommonname w/ 1carbonscellulosepolysaccharidewith all glucose,beta 1-4 bonds,and no branchpointscarboxylicacidderivativesacidchloride,acidanhydride,and amidelactosedisaccharidewith 2glucose +galactosebrainsugargalactoseis knownas a:acidicpolysaccharideheparinandhyaluronicacid are:reducingsugarsugar withfreeanomericcarbon(sucrose)decarboxylationremovesa CO2from themoleculesucrosedisaccharidewith glucose+ fructosesilvermirrorformationpositiveTollen'stestpropionaldehydealdehydecommonname w/ 3carbons-onesuffixused fornamingketonesacetalcontains 2 -OR groupson samecarbon-oatesuffix foracylportion ofan esterL-enantiomerhas -OHon left sideof FisherprojectionCH2OHpointsdownhow to IDthe L-enantiomerfor cycliccarbsketoacidpolyfunctionalacid withcarbonylgroupalphaanomeranomericcarbonpointsdowncellobiosedisaccharidewith 2glucosesand beta1-4linkagehemiacetalcontains -OH and -ORon samecarbon-oicacidsuffixforCOOHcarboxylicacid saltproductwhen COOHreacts w/ astrong basecarbonylcompoundshave anon-polarC-Z bond

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