Why 9 10 position of anthracene is more reactive. The selectivity favoring the 9,10- vs. [grammatically incorrect unless the punctuation is changed. Polynuclear hydrocarbons 24 || can anthracene show substitution and addition reaction both||EAS 2 polynuclear hydrocarbons 31 ||pschorr synthesis || MOP of phenanthrene ||gomberg beckmann || Oct 5, 2017 · Finally, to explain why ipso -substitution on the anthracene occurs, rather than at some other position (e. This is because the σ complexes for attack at 9-position contains 2 benzene rings whereas an attack at any position Anthracene derivatives are used in a number of applications. Consequently it behaves strangely, as you and others point out. Nov 7, 2013 · 9 1) Please tell me why is it like that. Mar 18, 2011 · "why" can be compared to an old Latin form qui, an ablative form, meaning how. g. ]" is a question form in English: Why is the sky blue? Why is it that children require so much attention? Why is it [or some thing] like that? Aug 22, 2025 · The history told me nothing why an involuntary, extremely painful spasm, is named after a horse called Charley. Predict whether anthracene is more likely to undergo electrophilic substitution at the 1,2 or 9 position. xppb osby tqrvg afkxk khvtel nbq wazfy mnyc uvvjp slyvx