Origin of the reactivity of allyl chloride and .alpha.-chloroacetaldehyde in SN2 nucleophilic substitution reactions: a theoretical comparison
β Scribed by Bach, Robert D.; Coddens, Barry A.; Wolber, Gregory J.
- Book ID
- 127046954
- Publisher
- American Chemical Society
- Year
- 1986
- Tongue
- English
- Weight
- 489 KB
- Volume
- 51
- Category
- Article
- ISSN
- 0022-3263
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π SIMILAR VOLUMES
The nucleophilic substitution in poly(viny1 chloride) (PVC) with sodium benzenethiolate has been studied in two kinds of solvent differing in the molecular structure in the vicinity of the carbonyl group. From the evolution of the content of isotactic (mm), heterotactic (mr), and syndiotactic (rr) t
Nucleophilic Substitution at a Trigonal Carbon. Part 6. Substituent and Bromide/Chloride Leaving Group Effects in the Reactions of Aromatic Acyl Chlorides with Methanol in Acetonitrile. -Investigation of the kinetics of methanolysis of benzoyl chloride and derivatives (I) shows that the chlorides f