Answer:
Cd2+ : 1s2 2s2 2p6 3s2 3p6 4s2 3d10 4p6 4d10 or [Kr] 4d¹⁰
Explanation:
Before proceeding to write out the electron configuration of Cd2+, we have to obtain the electron configuration of Cadmium (Cd),
Cadmium has an atomic number of 48, this means that a neutral cadmium atom will have a total of 48 electrons surrounding its nucleus.
The electronic configuration of Cadmium is;
Cd: 1s2 2s2 2p6 3s2 3p6 4s2 3d10 4p6 5s2 4d10
The shorthand notation is given as;
Cd: [Kr] 4d¹⁰5s²
Cd2+ means that it has two less electrons, hence it's electron configuration is given as;
Cd2+ : 1s2 2s2 2p6 3s2 3p6 4s2 3d10 4p6 4d10 or [Kr] 4d¹⁰
<em>Thermal energy</em> is the sum of the kinetic and potential energies of all the particles in an object.
Assume that you have 250 gL of water and 1 kg of water at the same temperature.
Then, each water molecule has the same kinetic energy.
The larger sample contains four times as many molecules, so it contains four times as much thermal energy.
Thus, thermal energy is directly proportional to mass.
In symbols, <em>KE </em>∝ <em>m</em> or <em>KE = km</em>.
The graph of a direct proportion is a <em>straight line passing trough the origin</em>.
It should look something like the graph below.
Answer:
8
Explanation:
the number before the abbrviation for calcium (Ca) shows how many calcium there is.
Answer:
The carbocation intermediate reacts with a nucleophile to form the addition product.
Explanation:
The reaction of benzene with an electrophile is an electrophillic substitution reaction. Here the electrophile replaces hydrogen. There is no formation of carbocation as intermediate in the reaction. Infact there is transition state where the electorphile attacks on benzene ring and at the same time the hydrogen gets removed from the benzene. So a transition carbocation is formed.
The general mechanism is shown in the figure.
i) Attack of the electrophile on the benzene (which is the nucleophile)
ii) The carbocation intermediate loses a proton from the carbon bonded to the electrophile.
iii) the carbocation formation is the rate determining step.
iv) There is no formation of addition product.
Thus the wrong statement is
The carbocation intermediate reacts with a nucleophile to form the addition product.