hydroxyacidspolyfunctionalacid withhydroxylgroupalditolreductionof sugarproducesan:storagepolysaccharidesstarchandglycogenare:milksugarlactoseis knownas a:maltosedisaccharidewith 2glucosesand alpha 1-4 linkageL-enantiomerhas -OHon left sideof Fisherprojectionaldohexosecarb withaldehydeand 6carbons-alsuffixused fornamingaldehydesbutyraldehydealdehydecommonname w/ 4carbonsamylosepolysaccharidewith all glucose,alpha 1-4bonds, and nobranch pointsesterproductwhen COOHreacts w/ analcoholsilvermirrorformationpositiveTollen'stestaldonicacidweakoxidation ofsugarproduces an:formaldehydealdehydecommonname w/ 1carbonsbrainsugargalactoseis knownas a:carboxylicacidproductwhenoxidize analdehydetest foraldehydesBenedict'sTestcarboxylateionproductwhen COOHreacts w/waterreducingsugarsugar withfreeanomericcarbon(sucrose)-oatesuffix foracylportion ofan estercellulosepolysaccharidewith all glucose,beta 1-4 bonds,and no branchpointsstructuralpolysaccharidescelluloseand chitinare:aldehydeproductwhen oxidizea primaryalcoholsaponificationhydrolysisof esterunder basicconditionscarboxylicacid saltproductwhen COOHreacts w/ astrong basecellobiosedisaccharidewith 2glucosesand beta1-4linkagecarboxylicacidderivativesacidchloride,acidanhydride,and amideD-enantiomerbiologicallyrelevantcarbohydrates-oicacidsuffixforCOOHformicacidcommonname forCOOH w/1 carbonCOOHabbreviationfor acarboxylicacidsecondaryalcoholproductwhenketone isreducedacidicpolysaccharideheparinandhyaluronicacid are:CH2OHpointsuphow to IDthe D-enantiomerfor cycliccarbsdecarboxylationremovesa CO2from themoleculeCH2OHpointsdownhow to IDthe L-enantiomerfor cycliccarbscarbonylcompoundshave anon-polarC-Z bondenantiomersnon-superimposablemirror imagesamylopectinpolysaccharidewith all glucose,alpha 1-4bonds, andsome alpha 1-6branch pointsketoacidpolyfunctionalacid withcarbonylgroupsucrosedisaccharidewith glucose+ fructosechiralcarbon w/4 differentgroupsketopentosecarb withketoneand 5carbonsalphaanomeranomericcarbonpointsdownacetaldehydealdehydecommonname w/ 2carbonsaceticacidcommonname forCOOH w/2 carbonsacetalcontains 2 -OR groupson samecarbonalwaysfound at endof parentchainCOOHand CHOgroupsare:unsaturatedacidpolyfunctionalacid withdouble bondslactosedisaccharidewith 2glucose +galactose-onesuffixused fornamingketoneshemiacetalcontains -OH and -ORon samecarbonaldaricacidstrongoxidation ofsugarproduces an:diastereomersisomersthat arenot mirrorimagespropionaldehydealdehydecommonname w/ 3carbonsacylcompoundshave apolar C-Z bondvalericacidcommonname forCOOH w/5 carbonsbetaanomeranomericcarbonpointsdownhydroxyacidspolyfunctionalacid withhydroxylgroupalditolreductionof sugarproducesan:storagepolysaccharidesstarchandglycogenare:milksugarlactoseis knownas a:maltosedisaccharidewith 2glucosesand alpha 1-4 linkageL-enantiomerhas -OHon left sideof Fisherprojectionaldohexosecarb withaldehydeand 6carbons-alsuffixused fornamingaldehydesbutyraldehydealdehydecommonname w/ 4carbonsamylosepolysaccharidewith all glucose,alpha 1-4bonds, and nobranch pointsesterproductwhen COOHreacts w/ analcoholsilvermirrorformationpositiveTollen'stestaldonicacidweakoxidation ofsugarproduces an:formaldehydealdehydecommonname w/ 1carbonsbrainsugargalactoseis knownas a:carboxylicacidproductwhenoxidize analdehydetest foraldehydesBenedict'sTestcarboxylateionproductwhen COOHreacts w/waterreducingsugarsugar withfreeanomericcarbon(sucrose)-oatesuffix foracylportion ofan estercellulosepolysaccharidewith all glucose,beta 1-4 bonds,and no branchpointsstructuralpolysaccharidescelluloseand chitinare:aldehydeproductwhen oxidizea primaryalcoholsaponificationhydrolysisof esterunder basicconditionscarboxylicacid saltproductwhen COOHreacts w/ astrong basecellobiosedisaccharidewith 2glucosesand beta1-4linkagecarboxylicacidderivativesacidchloride,acidanhydride,and amideD-enantiomerbiologicallyrelevantcarbohydrates-oicacidsuffixforCOOHformicacidcommonname forCOOH w/1 carbonCOOHabbreviationfor acarboxylicacidsecondaryalcoholproductwhenketone isreducedacidicpolysaccharideheparinandhyaluronicacid are:CH2OHpointsuphow to IDthe D-enantiomerfor cycliccarbsdecarboxylationremovesa CO2from themoleculeCH2OHpointsdownhow to IDthe L-enantiomerfor cycliccarbscarbonylcompoundshave anon-polarC-Z bondenantiomersnon-superimposablemirror imagesamylopectinpolysaccharidewith all glucose,alpha 1-4bonds, andsome alpha 1-6branch pointsketoacidpolyfunctionalacid withcarbonylgroupsucrosedisaccharidewith glucose+ fructosechiralcarbon w/4 differentgroupsketopentosecarb withketoneand 5carbonsalphaanomeranomericcarbonpointsdownacetaldehydealdehydecommonname w/ 2carbonsaceticacidcommonname forCOOH w/2 carbonsacetalcontains 2 -OR groupson samecarbonalwaysfound at endof parentchainCOOHand CHOgroupsare:unsaturatedacidpolyfunctionalacid withdouble bondslactosedisaccharidewith 2glucose +galactose-onesuffixused fornamingketoneshemiacetalcontains -OH and -ORon samecarbonaldaricacidstrongoxidation ofsugarproduces an:diastereomersisomersthat arenot mirrorimagespropionaldehydealdehydecommonname w/ 3carbonsacylcompoundshave apolar C-Z bondvalericacidcommonname forCOOH w/5 carbonsbetaanomeranomericcarbonpointsdown

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