Packet G: Tossup 6
TOAC (“T-O-A-C”) is a cyclic, radical one of these compounds used as a spin label in EPR spectroscopy. Isotope-labeled versions of these compounds are used in SILAC (“SYE-lack”) experiments. Derivatives of one of these compounds react with boroxines (“bor-OCK-seens”) to form asymmetric Corey–Bakshi–Shibata catalysts. These compounds are conjugated onto Wang resins using coupling agents like benzotriazoles or carbodiimides (“carbo-die-IM-mydes”) in Merrifield solid-phase synthesis. In that method, these compounds must be protected by groups like Boc (“bock”) and Fmoc (“F-mock”). These compounds are formed by treating an aldehyde with hydrogen cyanide then hydrolysis during the Strecker synthesis. Simple examples of these compounds can be formed by electrical discharges, as demonstrated by Miller and Urey. For 10 points, name these building blocks for polypeptides. ■END■
Buzzes
Summary
| Tournament | Edition | Match | Heard | Conv. % | Neg % | Avg. Buzz |
|---|---|---|---|---|---|---|
| California (North) | Main Site | ✓ | 3 | 100% | 33% | 111.33 |
| California (South) | Main Site | ✓ | 4 | 100% | 50% | 95.50 |
| Canada | Main Site | ✓ | 11 | 82% | 9% | 82.00 |
| Florida | Main Site | ✓ | 3 | 100% | 0% | 89.33 |
| Great Lakes | Main Site | ✓ | 5 | 100% | 20% | 86.60 |
| Lower Mid-Atlantic | Main Site | ✓ | 9 | 100% | 0% | 101.44 |
| Midwest | Main Site | ✓ | 8 | 100% | 25% | 88.63 |
| Northeast | Main Site | ✓ | 6 | 100% | 0% | 78.83 |
| Overflow | Main Site | ✓ | 4 | 100% | 25% | 91.75 |
| South Central | Main Site | ✓ | 2 | 100% | 0% | 86.50 |
| Southeast | Main Site | ✓ | 8 | 100% | 0% | 85.50 |
| UK | Main Site | ✓ | 12 | 100% | 33% | 84.92 |
| Upstate NY | Main Site | ✓ | 4 | 100% | 0% | 94.25 |