The reaction conditions to carry out the production of cyclopentene using bromocyclopentane as the starting material would be:
a. KOH, CH3CH2OH
b. H2SO4, THF
c. H2O2, OH
d. Hg(OAc)2,H2O
Question 2
Which of the following is a correct statement regarding electrophilic aromatic substitution?
a. The carbocation intermediate will lose a proton to regain aromaticity, usually from a position other than the site of electrophilic attack.
b. Formation of the carbocation intermediate has a high activation barrier due to loss of aromaticity.
c. The carbocation intermediate has several resonance structures and is negatively charged.
d. Re-formation of the aromatic ring has a low activation barrier and therefore occurs slowly.
e. Many suitable electrophiles are unreactive and can be stored for long periods of time prior to use.
A peroxidation reaction involving a fatty acid is depicted in the figure below.
(a) A photograph of a radial immunodiffusion reaction for measurement of patient IgA concentrations. ...
Hill plots of oxygen binding for myoglobin and hemoglobin under physiological conditions
Isomerization reaction proceeds via an enediolate intermediate.
If 250. L of nitrogen reacts with 582 L of hydrogen by the reaction: N2(g) + 3 H2(g) 2 NH3(g), ...
reaction