For the reaction below: a Draw the structure of the major organic product. (Do not include diisopropylamine.) Move Clear Erase Undo Redo Increase Scale Decrease Scale Copy Paste Set Label More Labels Attributes More Attributes Single Bond Recessed Bond Protruding Bond Double Bond Other Bond More Bonds Cyclohexane Ring Benzene Ring Other Ring More Rings Bracket Correct Owing to the high basicity of the enolate nucleophile, this alkylation is practical only with methyl and primary alkylating agents. For secondary and tertiary substrates, E2 elimination is the favored pathway. Multiple alkylation can be a significant side reaction. b Write the mechanism of the following reaction step using curved arrows to show electron reorganization.

c. because step up transformer steps up the input voltage i.e increases the input voltage  

the number of turns are greater on the secondary side of step up transformer  

transformer does not handle dc current

explanation:

let the different atoms be x and y. each with four protons and same mass will be represented as follows.

mass number is number of protons + number of neutrons.

            and  

since, it is given that one has a negative charge while the other is neutral. therefore, there will be increase in number of protons and the atom will be represented as follows.

according to periodic table, mass number of beryllium is 9 and it has atomic number 4 so, the atoms will be and .  

the protons and neutrons will be located inside the nucleus whereas the electrons will be revolving around the nucleus.