In orbitals diagrams, the **orbitals **are shown as** boxes,** and **the electrons **in them as** arrows** pointing up or down. Each box represents one orbital, and each arrow indicates one electron. This is a way of showing the electron configuration of the atom.

For example, the orbital diagram of Li can be shown as:

Just like in writing electron configurations, remember that **each orbital**, whether it is *s*, *p*, *d*, or *f* can accommodate **two electrons at most**, so you cannot put more than two arrows in a box.

Notice that if there are two electrons in the orbital, the **arrows must be shown in opposite directions** which indicates that they must have opposite spins. This is according to the **Pauli exclusion principle** which states that no two electrons in an atom can have the same four quantum numbers. So, if the electrons are in the same orbital, they must have the same *n*, *l*, *m*_{l}, and therefore, the only one that can be different is the *m*_{s} which is the spin of the electron shown by the position of the arrow.

Next, remember the **number and capacity** of *s*, *p*, *d*, and *f* are energy sublevels There can only be **1 s** orbital in the given energy level,

**3**,

*p*orbitals**5**, and

*d*orbitals**7**. And because each orbital can only take a maximum of two electrons, there can only be a maximum of

*f*orbitals**two electrons**in any

**,**

*s*sublevel**in the**

*6*electrons**,**

*p*subshell**10 in the**, and

*d***14 in the**.

*f*sublevel

Everything we discussed in the article about electron configurations holds true, so if you have forgotten things like the Aufbau Principle, and the orbital map to easily recognize what orbitals a given element has, check the linked article.

Remember, the order of filling the orbital goes from the lowest energy level to the highest considering the position of sublevels (*s*, *p*, *d,* *f*) as well.

Let’s now do some examples of electron configurations and how orbital diagrams represent them. First is the **hydrogen**, and it is in the first row, therefore, the only electron it has is going to be in the 1*s* level, and the electron configuration will be 1*s*^{1}:

^{ }

For the He, it will be 1s^{2} because it has two electrons, and the s orbital can still accommodate one more electron.

Next, we have lithium. Now, it is in the second row, but before getting there, we must use the 1s orbital. Remember, water couldn’t jump up without filling the lower levels. So, lithium has 3 electrons (atomic number), and therefore, the electron configuration will be 1s^{2}2s^{1}.

Consequently, Be will have one more electron with a configuration of 1s^{2}2s^{2}.

Next, we have boron, and it is in the region of *p* orbitals. Therefore, everything we had for Be, is still going to be in place, and the one additional electron will go to the 2p orbital:

Now, carbon is going to add one more electron in the p sublevel thus having 1*s*^{2}2*s*^{2}2*p*^{2} electron configuration. What is important is that this electron goes to the **next** (**empty**) *p* orbital rather than fitting in with the other electron:

This is the **Hund’s rule**, which states that **electrons will fill** all the degenerate orbitals (equal in energy) with **parallel spins (both arrows up or down) first** before pairing up in one orbital. We can also formulate it as the lowest energy configuration for an atom is the one having the **maximum number of unpaired electrons** within the **same energy sublevel. **

**Hund’s rule **is another demonstration of the same principle which is the **tendency to adopt the lowest energy** state possible. There is a stronger repulsive interaction between two electrons in the same orbital compared to when they occupy separate orbitals of equal energy.

So, as expected, the next element, nitrogen will place the additional electron in the 3^{rd} *p* orbital which is empty in carbon.

Following the same principle, we get to Ne which has a complete filling of the *n *= 2 principal level.

Now, there is something special about (completely)** filled orbitals**. This makes the electrons very low in energy meaning they are **stable** and cannot normally lower their energy more by participating in chemical reactions. Therefore, Ne and all the other noble gases below it, are the **most chemically stable** and thus **unreactive** (**inert**) family in the periodic table.

The first element in period 3 is sodium, Na, and we are going to write the electron configuration of Ne with an additional electron in the 3s sublevel:

**Writing an Electron Configuration for an Element from Its Position in the Periodic Table**** **

At some point, when start noticing the pattern of filling the orbitals, and their mapping on the periodic table, it may be easier to write the electron configuration simply based on the position of the element. So, instead of starting from 1*s*^{2}…., we **write the electron configuration of the last noble gas** that comes before the element and then **add the remaining electrons** from the corresponding *n* level. **For example**, let’s say we want to write an electron configuration for **sulfur**. First, you need to write the inner electron configuration, that is the configuration of the noble gas that precedes it in the periodic table. In this case, it is Ne, and since it is in the last element in the second row, the last filled sublevel would be 2p^{6}, and therefore, the electron configuration of the noble gas will be 1*s*^{2}2*s*^{2}2*p*^{6}. Now, to this, we add **2 s** electrons, and

**four**electrons since S is the fourth element in the p orbital area:

*p*

Therefore, the electron configuration will be 1*s*^{2}2*s*^{2}2*p*^{6}3*s*^{2}2*p*^{4}.

** **

**Condensed electron configurations **

In condensed electron configurations, we show the **symbol of the noble gas that precedes the element** in square brackets, and then **add the remaining electrons** just as we have been doing so far. So, for the sulfur, it will be S: **[Ne]3 s^{2}2p^{4}**.

**Another example** is the electron configuration of Br. Since it is in the 4^{th} row, the **inner configuration** would be that of **Ar**, and after that, we add the electrons as we did for the d elements that we have discussed. Two electrons will go into the 4*s* orbital, 10 to the 3*d* orbitals, and 5 into the 4p sublevel – **Br: [Ar]4 s^{2}3d^{10}4p^{5}**.

**Electron Configuration of ***d* Elements – the Transition Series

*d*Elements – the Transition Series

There is one exception to keep in mind for the electron configuration of transition metals. That is the **( n +1)s** orbitals always

**fill before**the

*n*d orbitals.For example, the 4s level fills before the 3d level, and therefore, the electron configuration of Ti is 1*s*^{²}2*s*^{²}2*p*^{⁶}3*s*^{²}3*p*^{⁶}4*s*^{²}3*d*^{² }or, the condensed configuration which will be [Ar]4*s*^{²}3*d*^{²}.

As we get to higher values of *n, o*ther variations in the filling pattern occur because the energy sublevels become very close together (recall the figure on the energy levels above).

**Stability of Half-Filled and Filled Sublevels **

We mentioned that noble gases are characterized by great stability because of their completely filled orbitals. Now, similar to this, orbitals tend to get lower energy levels (high stability) when they are **half-filled**. For example, following what we have learned so far, we may expect the following electron configuration for Cr: [Ar]4*s*^{²}3*d*^{4}.

However, the **electron configuration of Cr is [Ar]4 s^{1}3d^{5}**, and the reason for this is that the

*d*orbital gets a

**half-filled configuration**(remember d orbitals can have a maximum of 10 electrons). We can think of this as the electron jumping from the 4

*s*level to the 3d level and compensating this energy uphill by a stabilization associated with half-filled orbitals:

Of course, in reality, it is not as though the electrons fill one by one, and then one of them jumps from 4s to 3d level. However, this is a visual representation to help better understand this behavior in the electron configuration of transition elements.

Let’s also discuss the **electron configuration of Cu** which stands before Zn, and one may expect it to have 9 electrons in the d sublevel. However, the correct electron configuration of **Cu** is [Ar]**4 s^{1}3d^{10}** as this allows to attain

**filled**and a

*d*orbitals**half-filled**which is lower in energy (

*s*orbital**more stable**) than the expected [Ar]4

*s*

^{2}3

*d*

^{9}configuration.

**Inner Transition Series (***f* Elements)

*f*Elements)

Starting from period 6, we have the **inner transition elements** which contain *f *orbitals. The first thing you need to remember here is that there are **seven f orbitals** because

*l*= 3, so the possible

*ml*values are −3, −2, −1, 0, +1, +2, and +3. Each orbital can accommodate two electrons and therefore,

**a total of 14 electrons**can fill the given f sublevel.

Although the first element in this region is La, the filling of *f* orbitals starts from Cerium (Ce), and the elements together with it in the Period 6 are called **lanthanides **(or **rare earth **elements).

Notice the general filling order is 6s → 4f → 5d, however, *ns* goes first, then **only the first** of (*n *− 1)*d, *all (*n *− 2)*f, and after that *remainder of the (*n *− 1)*d*, and *np. *Therefore, the electron configuration of La is [Xe]6s^{²}5d^{¹} and not [Xe]6s^{²}4f^{¹} as the first d electron goes first.

The inner transition series in Period 7 start after actinium (Ac; *Z *= 89) and are called the **actinides.**

Hopefully, you won’t get tested on remembering all these exceptions as it should be the principle that is more important, but in any case, use the ptable.com website to practice filling electron configurations. Just be sure to click the “Electrons” tab in the upper area.

**Valence Electrons and Electron Configurations**

Valence electrons are the ones farthest away from the nuclei and therefore, we find them in the outermost two orbitals. For example, Li (1*s*^{2}2*s*** ^{1}**) has one valence electron, and it is the 2

*s*orbital. Chlorine (1

*s*

^{²}2

*s*

^{²}2

*p*

^{⁶}3

*s*

^{²}3

*p*

^{⁵}) has seven valence electrons in the 3

*s*and 3

*p*sublevels. If you ever forget, remember that you can easily double-check this based on the group number. The

**group number**indicates the

**number of valence electrons**in the atom.

**Electron Configuration of Ions**

The first thing you need to remember here is that cations are formed by losing an electron(s), and anions are forming by gaining an electron(s).

The **charge of the ion is a result of an imbalance between the number of protons** and electrons. If it is a **cation**, then the positive indicates how many **more protons** it has compared to the number of electrons. For **anions**, the charge tells how many **extra electrons **there are compared to the number of protons.

Recall, this pattern for the formation of anions and cations: Metals tend to lose electron(s) and become **cations** (positively charged ions).

Nonmetals tend to gain an electron(s) and become **anions** (negatively charged ions).

Notice that the number of protons is not changed, and the **ions** are charged because, unlike atoms, their number of **protons and electrons is not equal**.

**Orbital Diagrams**** of Main Group Cations**

Now, how do we determine the electron configuration of an ion? If it is, for example, a **+1 charged** cation, that means the atom has **lost one electron**. This electron is **going to be from the outermost** **valence shell** as these are the electrons farthest away from the nuclei and thus not as strongly attracted to it.

Let’s see an **example on Na**. It is in the first group, so it **loses one electron** to become **Na ^{+}**. The electron configuration of sodium is 1

*s*

^{²}2

*s*

^{²}2

*p*

^{⁶}3

*s*

^{¹}, and the electron is removed from the energy level with the greatest n value – 3

*s*. Therefore, the electron configuration of the

**Na**ion will be

^{+}**1**:

*s*^{²}2*s*^{²}2*p*^{⁶}

Notice that the ion has a configuration with a **complete shell of p orbitals** which is characteristic of **noble gases**. In fact, this is the electron configuration of Ne, and we say that Na^{+} and Ne are **isoelectronic** (same electronic structure). The reason for this is that, remember, noble gases are very stable because of the low energy level of complete orbitals.

This pattern explains why the **metals in the first group become +1**, the ones in the **second group** become +2, and **Al**, for example, becomes **+3**. It takes removing one electron from a metal in the first group to obtain the electron configuration of the previous noble gas, it takes two for the group two metals, etc.

Na (1*s*^{2}2*s*^{2}2*p*^{6}3*s*^{1}) ⟶ e^{−} + **Na ^{+}**([He]2

*s*

^{2}2

*p*

^{6}) [

**isoelectronic with Ne**([He] 2

*s*

^{2}2

*p*

^{6})]

**Orbital Diagrams of Anions**

Anions are formed when the atom **gains as many electrons** as necessary to **attain the electron configuration of the next noble gas** in the periodic table. For example, **oxygen** is in group 6, and therefore, it will need **two electrons** to attain the electron configuration of Ne:

Notice again that the two electrons go to the outermost valence orbital. Oxygen has 6 valence electrons – those in the 2*s* and 2*p* orbitals, however, since p sublevels are higher in energy, and they are the only ones capable of accepting additional electrons, the two electrons go to the 2*p* orbitals. The electron configuration of the oxide ion (**O ^{2-}**) is therefore,

**1**.

*s*^{²}2*s*^{²}2*p*^{⁶}

O (1*s*^{2}2*s*^{2}2*p*^{4}) + 2e^{−}⟶ + O** ^{2- }**([He]2

*s*

^{2}2

*p*

^{6}) [

**isoelectronic with Ne**([He] 2

*s*

^{2}2

*p*

^{6})]

Another common type of monoatomic anions are the **halides**. Halogens are in **group 7**, and therefore, they **only need one electron** to attain the electron configuration of the noble gas following them in the periodic table. **For example**, bromine takes one electron and becomes isoelectronic to t Kr:

Br([Ar] 4*s*^{2}3*d*^{10}4*p*^{5}) + e^{− }⟶ **Br ^{−}**([Ar] 4

*s*

^{2}3

*d*

^{10}4

*p*

^{6}) [

**isoelectronic with Kr**([Ar] 4

*s*

^{2}3

*d*

^{10}4

*p*

^{6})]

**Orbital Diagrams**** of Transition Metal Cations**

In contrast to main-group ions, transition metal ions **do not usually attain a noble gas configuration**. This is because the ns level is the outermost level, and the (n-1)d is considered an inner level therefore, it will take too much energy to remove those electrons and achieve a noble gas configuration. Therefore, the cation of a transition metal is formed by removing **first the electrons from the n s** (highest principal quantum number) orbital and

**then from the (n -1)**orbitals.

*d*

**For example**, the **electron configuration of Zn** is 1s^{2}2s^{2}2p^{6}3s^{2}3p^{6}**4 s^{2}3d^{10}** or [Ar]

**4**, and it loses the two electrons from the 4s orbital to become Zn

*s*^{2}3*d*^{10}^{2+}[Ar]

**3**. This is “not a bad” electron configuration considering the filled d orbitals.

*d*^{10}** **

**Excited and Ground State Electron Configurations and ****Orbital Diagrams**

Remember, when discussing the Bohr model of the hydrogen atom, we mentioned that **absorbing** light with sufficient energy **moves the electron to a higher energy level**, and when it falls back **to a lower energy level**, light is **emitted** as energy is lost.

Now, when the **electron is in a higher energy** level than it normally is, the atom or ion is said to be in the **excited state**. If the electrons are in the **lowest possible energy** levels, the atom is in the **ground state**. So, everything we have discussed today pertains to the electron configurations of atoms at the ground state. In general, *unless mentioned otherwise*, the term electron configuration refers to the atom in the *ground state*.

**An example** of switching from the ground to an excited state can be when the electron in a carbon atom jumps from the 2*s* to the 2*p* level. The electron configurations and orbital diagrams can be represented as:

These electron transitions from lower to higher energy orbitals are the basis of many spectroscopies for determining the molecular structures in inorganic and organic materials.

**Check Also**

- Atomic Orbitals
- Electron Configurations
- Electron Configurations of Ions
- Aufbau’s Principle, Hund’s Rule, and Pauli’s Exclusion Principle
- Hund’s Rule
- Pauli Exclusion Principle
- Quantum Numbers (
*n*,*l*,*m*_{l},*m*_{s}) - Bohr Model of the Hydrogen Atom
- Rydberg Formula
- The Photoelectric Effect
- Calculating The Energy of a Photon
- Ionization Energy
- Electron Affinity
**Energy, Wavelength, and Frequency Practice Problems**

#### Practice

What is the maximum number of electrons that can occupy one p orbital?

a.14

b. 2

c. 10

d.1

e. 6

The n = 2 shell can accommodate a maximum of ____ electrons.

A. 10

B. 8

C. 4

D. 6

E. 2

Which of the following is an incorrect orbital occupancy representation?

- 4d
^{3} - 3d
^{5} - 2s
^{3} - 1s
^{1} - 2p
^{2}

The maximum number of electrons that can be accommodated in 3s subshell is

- 10
- 2
- 6
- 1
- 8

The following electron configuration is incorrect:

- 1s
^{2}2s^{2} - 1s
^{2}2s^{3}2p^{3} - 1s
^{2}2s^{2}2p^{5} - 1s
^{2}2s^{2}2p^{4} - 1s
^{2}2s^{2}2p^{6}3s^{2}

Which electron configuration represents an excited state of the indicated atom?

**He**: 1s^{2}**Na**: 1s^{2}2s^{2 }2p^{6}3s^{2}3p^{2}3s^{1}**P**: 1s^{2}2s^{2}2p^{6}3s^{2 }3p^{3}**N**: 1s^{2}2s^{2 }2p^{2}3s^{1}**Ne**: 1s^{2}2s^{2}2p^{6}

Which of the following represents the ground state electron configuration of a transition element?

- 1s
^{2}2s^{2}2p^{6}3s^{2}3p^{5} - 1s
^{2}2s^{2}2p^{6}3s^{2}3p^{6}3d^{10}4s^{1} - 1s
^{2}2s^{2}2p^{6}3s^{2}3p^{6}3d^{10}4s^{2}4p^{4} - 1s
^{2}2s^{2}2p^{6}3s^{2}3p^{6}4s^{2} - 1s
^{2}2s^{2}2p^{3}

Which of the following is the correct ground-state electron configuration of V is?

- 1s
^{2}2s^{2}2p^{6}3s^{2}3p^{6}3d^{3} - 1s
^{2}2s^{2}2p^{6}3s^{2}3p^{6}3d^{5} - 1s
^{2}2s^{2}2p^{6}3s^{2}4s^{2}3d^{3} - 1s
^{2}2s^{2}2p^{6}3s^{2}3p^{6}4s^{2}3d^{5} - 1s
^{2}2s^{2}2p^{6}3s^{2}3p^{6}4s^{2}3d^{3}

Which of the following represents a possible excited-state electron configuration for an iron atom?

- [Ar]3d
^{7}4s^{2} - [Ar]3d
^{6}4s^{2} - [Ar]3d
^{7}4s^{1} - [Ar]3d
^{6}4s^{1} - [Kr]3d
^{7}4s^{1}

Each of the following is an accurate representation of ground-state electron configuration except:

**Fe**: [Ar]4s^{2}3d^{6}.**Ca**: [Ar]4s^{2}.**Se**: [Ar] 4s^{2}3d^{10}4p^{4}.**Ag**: [Kr] 5s^{2}4d^{9}.**Ti**: [Ar] 4s^{2}3d^{2}

How many electrons, in total, are present in p orbitals in a ground-state nickel atom?

- 8
- 12
- 6
- 24
- 3

Which one of the following represents electron configuration of an excited carbon atom?

- 1s
^{2}2s^{2}2p^{3} - 1s
^{2}2s^{2}2p^{1} - 1s
^{2}2s^{2}2p^{1}3s^{1} - 1s
^{2}2s^{2}3s^{1} - 1s
^{2}2s^{2}2p^{2}

Which of the following ground-state electron configurations is incorrect?

**Cl**: [Ne]3s^{2}3p^{5}**Ge**: [Ar] 4s^{2 }3d^{10}3p^{2}**Co**: [Ar]4s^{2}3d^{7}**Rb**: [Kr]5s^{1}**Mn**: [Ar] 4s^{2}3d^{5}

What is the ground-state electron configuration of chromium (Cr)?

- 1s
^{2}2s^{2}2p^{6}3s^{2}3p^{6}3d^{10}4s^{2}4p^{6}4d^{10}5s^{2}5p^{4} - 1s
^{2}2s^{2}2p^{6}3s^{2}3p^{6}4s^{1}3d^{5} - 1s
^{2}2s^{2}2p^{6}3s^{2}3p^{6}3d^{10} - 1s
^{2}2s^{2 }2p^{6}3s^{2}3p^{6}4s^{2}3d^{4} - 1s
^{2}2s^{2}2p^{6}3s^{2}3p^{6}3d^{6}

What is the ground-state electron configuration of bromine (Br)?

- 1s
^{2}2s^{2}2p^{6}3s^{2}3p^{6}4s^{1}3d^{10 }4p^{5} - [Kr] 4s
^{2}3s^{10}4p^{5} - [Ne] 3s
^{2}3p^{5} - [Ar] 4s
^{2}3d^{10}4p^{5} - 1s
^{2}2s^{2}2p^{5}3s^{2}3p^{6}4s^{2}3d^{10}4p^{5}

The ground state electron configuration of As is ________.

- 1s
^{2}2s^{2}3s^{2}3p^{6}4s^{2}3d^{10}4p^{2} - 1s
^{2}2s^{2}2p^{6}3s^{2}3p^{6}4s^{2}3d^{10}4p^{1} - 1s
^{2}2s^{2}2p^{6}3s^{2}3p^{6}4s^{2}3d^{10}4p^{3} - 1s
^{2}2s^{2}2p^{6}3s^{2}3p^{6}4s^{2}3d^{10}4d^{3} - [Kr]4s
^{2}3d^{10}4d^{3}

Which of the following elements has the same valence-shell electron configuration as lithium?

- calcium.
- sulfur.
- potassium.
- magnesium.
- argon.

How many unpaired electrons are found in the d orbital of nickel.

- 4 electrons
- 3 electrons
- 2 electrons
- 8 electrons
- none of these

The ground-state electron configuration of the element ________ is [Kr]5s^{2}4d^{10}

- Fe
- Cd
- Cr
- Mn
- Zn

The ground-state electron configuration of ________ is [Ar]4s^{2}3d^{7}.

- Ti
- Co
- Fe
- Cr
- Cs

Chlorine has the following ground-state configuration:

- [He]3s
^{2}3p^{2} - [Ne]3s
^{2}3p^{5} - [He]2s
^{2}2p^{5} - [Ne]2s
^{2}2p^{3} - [He]3s
^{2}3p^{5}

What is the maximum number of electrons that can be accommodated in each d-subshell?

- 10
- 5
- 6
- 3
- 2

What noble gas core should be used when writing the condensed electron configuration of Strontium (Sr)?

- [Xe]
- [Kr]
- [Ne]
- [Ar]
- [He]

# Electron Configuration of Ions

Which of the following is the ground state electron configuration of S^{2-}?

A) [Ne]

B) [Ne]3s^{2}3p^{6 }C) [Ne]3s^{2}3p^{4 }D) [Ne]3s^{2}3p^{2 }E) [Ne]4s^{2}

A cation of +3 indicates that an element has

A) lost three neutrons.

B) lost three protons.

C) lost three electrons.

D) gained three protons.

E) gained three electrons.

Indicate the ground state electron configuration for Cl⁻.

A) 1s^{2}2s^{2}2p^{6}3s^{2}3p^{4 }B) 1s^{2}2s^{2}2p^{6}3s^{2}3p^{5 }C) 1s^{2}2s^{2}2p^{6}3s^{2}3p^{6 }D) 1s^{2}2s^{2}2p^{6}3s^{1}3p^{6 }E) 1s^{2}2s^{2}2p^{6}3s^{3}3p^{5}

Which of the following is the ground state electron configuration of Ba^{2+ }?

A) [Kr]5s^{2}4d^{10}5p^{6}6s^{2 }B) [Kr]5s^{2}4d^{10}5p^{6 }C) [Kr]5s^{2}4d^{10}5p^{6}5d^{2 }D) [Kr]5s^{2}5p^{6 }E) [Kr]5s^{2}4d^{10}5p^{6}6s^{2}

Which of the following is the ground state electron configuration of Ti^{2⁺}.

A) [Ar]3d^{4 }B) [Ar]3d^{2 }C) [Ar]4s^{2 }D) [Ar]4s^{2}3d^{4 }E) [Ar]4s^{2}3d^{2}

Which of the following is the ground state electron configuration of Zn^{2⁺}?

A) [Ar]4s^{2}3d^{6 }B) [Ar]3d^{10 }C) [Ar]4s^{2}3d^{8 }D) [Ar]3d^{8 }E) [Ar]

Which of the following is the ground state electron configuration of Cr^{3⁺}?

A) [Ar]

B) [Ar]4s^{1}3d^{2 }C) [Ar]3d^{3 }D) [Ar]4s^{2}3d^{1 }E) [Ar]4s^{2}3d^{7}

How many valence electrons are present in the azide (N^{3-}) ion?

A) 3

B) 5

C) 8

D) 7

E) 2

Ca^{2+} has the following ground state electron configuration:

A) 1s^{2}2s^{2}2p^{6 }B) 1s^{2}2s^{2}2p^{6}3s^{2 }C) 1s^{2}2s^{2}2p^{6}3s^{2}3p^{2 }D) 1s^{2}2s^{2}2p^{6}3s^{2}3p^{6}4s^{2}3d^{2 }E) 1s^{2}2s^{2}2p^{6}3s^{2}3p^{6}

Rb+ has the following ground state electron configuration:

A) [Kr]5s^{2}4d^{6 }B) [Kr]4s^{2 }C) [Ar]4s^{2}4p^{4 }D) [Kr]5s^{1 }E) [Ar]4s^{2}3d^{10}4p^{6}

Which of the following is the ground state electron configuration of Fe^{3⁺}?

A) [Ar]3d^{5}** ^{ }**B) [Ar]4s

^{1}3d

^{3 }C) [Ar]

D) [Ar]4s

^{2}3d

^{9 }E) [Ar]4s

^{2}3d

^{1}

The correct ground state electron configuration for Br^{–} is:

A) [Ar]4s^{2}3d^{10}4p^{6 }B) [Ar]4s^{2}3d^{10}4p^{3 }C) [Ar]4s^{2}3d^{8}4p^{6 }D) [Ar]4s^{2}3d^{10}4p^{5 }E) [Ar]4s^{2}4p^{6}

How many electrons are present in the ground state of Mg^{2+} ion?

A) 2

B) 6

C) 10

D) 8

E) 12