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Substituent effects in the photosolvolysis of benzyl derivatives. General structure-reactivity relationships.

✍ Scribed by Peter Wan; Becky Chak; Carrier Li

Publisher
Elsevier Science
Year
1986
Tongue
French
Weight
224 KB
Volume
27
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

✦ Synopsis

The relative reactivity of photosolvolysis of a number of substituted benzyl acetates is in the order ortho > meta > para, these substitutent effects being apparently additive, as suggested by the relative reactivity of photomethanolysis of several dimethoxy-substituted benzyl alcohols.

The photosolvolysis of benzyl systems has been an area of much interest.

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