explain why ethoxybenze is brominated more rapidly than phenyl benzoate
explain why ethoxybenze is brominated more rapidly than phenyl benzoate
Explain in detail why does bromination of ethoxy benzene occur more rapidly than phenyl benzoate? Please illustrate also.
At what position, and on what ring, is bromination of phenyl benzoate expected to occur? Show your product and explain your answer.
Explain why the temperature boundary layer grows much more rapidly than the velocity boundary layer for liquid metal?
1. Flammable substances will burn more rapidly in pure oxygen than in air. Explain why this happens 2. in terms of energy and bonds, explain what causes a reaction to be exothermic or endothermic. Do not simply tell what it means for a reaction to be exothermic or endothermic.
3. Explain why, in a chemical reaction, the concentration of a reactant decreases more rapidly at a lower time t than at a higher t.
Which of the position(s) shown is where a single bromination of phenyl benzoate expected to occur most often? Briefly explain your answer.
Why potassium permanganate and methylene blue dyes diffuse more rapidly through water than agar gel?
Why is water solubiilty of benzoic acid significantly less than the water solbilty of the benzoate ion? Briefly explain and relate to the partition coefficient (kD).
Numbers 1 and 2 What is the correct structure for phenyl benzoate? What is the order of decreasing reactivity towards nucleophilic acyl substitution for the carboxylic acid derivatives? (most reactive first). a. I, II, III, IV b. I, III, IV, II c. II, IV, III, I d. II, I, III, IV
Use these names: Acetanilide, Benzaldehyde, Benzophenone, Diphenylmethane, t-Butanol, Phenyl Benzoate, o-Toluic Acid, Phenol, and Acetophenone and their structural formulas to identify the functional groups/bond types in each