## Abstract The hydroxyl proton chemical shift in substituted benzyl alcohols may be used, either at infinite dilution in CCl~4~, or in dilute solutions in DMSO, as a reliable indicator of substituent effects. The sensitivity of the hydroxyl proton to substituents is much greater than that of the m
Hydroxyl Substituent Chemical Shift (SCS) Effects in Alcohols: The 17 O NMR of Diols
β Scribed by Alam, Todd M.; Click, Carol A.
- Book ID
- 120284422
- Publisher
- Taylor and Francis Group
- Year
- 1998
- Tongue
- English
- Weight
- 269 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0038-7010
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
There are many literature examples correlating C-13 n.m.r. substituent chemical shifts in substituted benzenes with Bsamett substituent constants.' The direction of these substituent chemical shifts has been logically explained in terms of substituent electronic properties; the electron donors resul
1998 magnetic resonance, nuclear quadrupole resonance magnetic resonance, nuclear quadrupole resonance (organic substances) K 2560 ## 09 -012 Proton Chemical Shifts in NMR. Part 10. Bromine and Iodine Substituent Chemical Shifts (SCS) and an Analysis of the Contributions to the SCS in Halocyclohex