Identify intermediate A, which has a molecular formula of C10H16O2, and give a curved-arrow mechanism for the transformation of A to the final product. Details count! Show ALL lone pairs of electrons and formal charges. Once you have supplied the organic intermediate A, do not add or remove atoms for the rest of the steps (i. e., atom conservation). If a CHx group is being deprotonated, draw all H\'s on the reacting site.

Select the correct answer from each drop-down menu.describe what happens to a carbon-11 atom when it undergoes positron emission.the decay of a carbon-11 atom _1_, and this causes it to emit _2_.options for 1: > changes a neutron into a proton> changes a proton into a neutron> is hit with a neutron> reconfigures its protons and neutronsoptions for 2: > a negatively charged electron-sized particle> a positively charged election-sized particle> two atoms and several neutrons> two neutrons and two protons