Kinetic studies on general base-catalyzed cleavage of phthalimide (PTH) in 2-hydroxyethylamine and 2-methoxyethylamine buffers
β Scribed by M. Niyaz Khan
- Book ID
- 102653035
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 547 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0538-8066
No coin nor oath required. For personal study only.
β¦ Synopsis
Kinetic studies on the nucleophilic cleavage of phthalirnide [ PTH) in buffers of 2-hydroxyethylarnine and 2-rnethoxyethylarnine reveal nonlinear plots of k, vs I Bufl, (at constant pH)
where k, and IBuf], represent apparent second-order rate constant and total arnine buffer concentration, respectively. The nonlinear variation of k, against [BuflT is attributed to the occurrence of a stepwise mechanism in the aminolysis of PTH Intermolecular general base catalysis is detected in the reactions of both arnines with nonionized PTH (SH) only within the pH range of the present study 0 1996 john Wiley &Sons, Inc
π SIMILAR VOLUMES
The effects of mixed CH 3 CN 9 H 2 O solvents on rates of aminolysis of ionized phenyl salicylate, PS Οͺ , reveal a nonlinear decrease in the nucleophilic second-order rate constants, (for aminolysis) with increase in the content of CH 3 CN until it becomes Ο· 50%, ms k , n v/v. The values of remain a
Nucleophilic second-order rate constants, k n ms , for the reactions of several primary and secondary amines with ionized phenyl salicylate (PS Οͺ ) show a nonlinear decrease with the increase in the content of CH 3 CN from 2 to Υ 50% v/v in mixed aqueous solvent. The values of k n ms remain almost un
Pseudo-first-order rate constants (k 1 ) for the reaction of ethane-1,2-diol (DOL) with ionized phenyl salicylate (PS Γ ), obtained in mixed DOL-CH 3 CN solvent at constant [H 2 O] and [NaOH], obey the relationship , where a is the apparent second-order rate constant, K A is the association constan