Packet E: Bonus 13

This functional group can be added to arenes (“AIR-eens”) using the Vilsmeier–Haack reagent, which is formed in situ from phosphorus oxychloride and DMF. For 10 points each:
[10h] Name this functional group added to phenols using chloroform and a strong base in the Reimer–Tiemann reaction. An industrial process for adding this functional group to alkenes uses rhodium complexed to sodium salts of sulfonated triphenylphosphine.
ANSWER: formyl group [accept formylation or hydroformylation; accept aldehyde; accept CHO or COH; prompt on carbonyl or CO] (The industrial process is the Ruhrchemie/Rhone–Poulenc process, and the ligand is TPPTS.)
[10m] Deprotonating chloroform generates these compounds for EAS (“E-A-S”) in the Reimer–Tiemann reaction. Lone pairs of the N-heterocyclic type of these compounds coordinate ruthenium in Grubbs catalysts used for olefin metathesis.
ANSWER: carbenes [accept N-heterocyclic carbenes or NHCs; accept persistent carbenes; accept dichlorocarbenes]
[10e] The Reimer–Tiemann reaction has largely supplanted Gattermann–Koch formylation for the production of salicylaldehyde (“SAL-uh-sill-aldehyde”) due to the latter’s use of this toxic gas that competes with O2 for binding to hemoglobin.
ANSWER: carbon monoxide [or CO]
<AL, Chemistry> | Packet E - Chicago A, Toronto B, Brandeis B, JHU A

HeardPPBE %M %H %
7510.1391%7%4%

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Conversion


Summary

TournamentEditionMatchHeardPPBE %M %H %
California (North)Main Site36.6767%0%0%
California (South)Main Site410.0075%25%0%
CanadaMain Site110.00100%0%0%
FloridaMain Site310.00100%0%0%
Great LakesMain Site510.00100%0%0%
Lower Mid-AtlanticMain Site98.8989%0%0%
MidwestMain Site811.25100%13%0%
NortheastMain Site510.0060%0%40%
OverflowMain Site410.00100%0%0%
South CentralMain Site210.00100%0%0%
SoutheastMain Site78.5786%0%0%
UKMain Site1210.8392%17%0%
Upper Mid-AtlanticMain Site812.50100%13%13%
Upstate NYMain Site410.00100%0%0%