Packet C: Bonus 8

A modification of this reaction typically uses a cyclic amine to catalyze the nucleophilic addition of an activated methylene into a carbonyl and was discovered by Emil Knoevenagel (“kuh-NO-vuh-NAH-gul”). For 10 points each:
[10m] Name this reaction described by the Zimmerman–Traxler model, which predicts that 1,3-allylic strain is minimized in its transition state. Unlike Claisen condensations, this reaction uses a ketone or aldehyde electrophile.
ANSWER: aldol reaction [or aldol condensation or aldol addition]
[10e] This property is maintained syn in aldol reactions according to the Zimmerman–Traxler model and can be controlled using Evans oxazolidinones (“ox-uh-ZO-lid-in-owns”). Compounds with this property cannot be superimposed on its mirror image.
ANSWER: chirality [or chiral; accept chiral auxiliaries; accept enantiomeric or enantioselectivity; prompt on stereometric or stereoselectivity; prompt on asymmetry or asymmetric induction; prompt on racemic; prompt on optical active or optical activity; prompt on isomerism]
[10h] The Zimmerman–Traxler model does not apply to Mukaiyama aldol reactions that use enol ethers of this functional group, which can be generated using the stereoretentive Brook rearrangement.
ANSWER: silyl groups [or silane groups; accept silyl ethers or silyl enol ethers; accept acylsilanes; accept trimethylsilyl groups or TMS groups; accept triethylsilyl groups or TES groups or tert-butyldimethylsilyl groups or TBS groups; prompt on organosilicon groups]
<Virginia Tech A, Chemistry> | Packet C - Virginia Tech A, Waterloo A, UCSD A, UBC A

HeardPPBE %M %H %
7214.0394%28%18%

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Conversion

TeamOpponentPart 1Part 2Part 3TotalParts
Central Florida ACentral Florida B1010020ME
Central Florida CFlorida A1010020ME
Florida CFlorida B010010E

Summary

TournamentEditionMatchHeardPPBE %M %H %
California (North)Main Site313.3367%67%0%
CanadaMain Site1013.0090%20%20%
FloridaMain Site316.67100%67%0%
Great LakesMain Site514.00100%20%20%
MidwestMain Site812.5075%25%25%
NortheastMain Site618.33100%50%33%
OverflowMain Site410.00100%0%0%
South CentralMain Site215.00100%50%0%
SoutheastMain Site714.29100%29%14%
UKMain Site1213.33100%25%8%
Upper Mid-AtlanticMain Site816.25100%25%38%
Upstate NYMain Site412.50100%0%25%