Answer:
a. electrophilic aromatic substitution
b. nucleophilic aromatic substitution
c. nucleophilic aromatic substitution
d. electrophilic aromatic substitution
e. nucleophilic aromatic substitution
f. electrophilic aromatic substitution
Explanation:
Electrophilic aromatic substitution is a type of chemical reaction where a hydrogen atom or a functional group that is attached to the aromatic ring is replaced by an electrophile. Electrophilic aromatic substitutions can be classified into five classes: 1-Halogenation: is the replacement of one or more hydrogen (H) atoms in an organic compound by a halogen such as, for example, bromine (bromination), chlorine (chlorination), etc; 2- Nitration: the replacement of H with a nitrate group (NO2); 3-Sulfonation: the replacement of H with a bisulfite (SO3H); 4-Friedel-CraftsAlkylation: the replacement of H with an alkyl group (R), and 5-Friedel-Crafts Acylation: the replacement of H with an acyl group (RCO). For example, the Benzene undergoes electrophilic substitution to produce a wide range of chemical compounds (chlorobenzene, nitrobenzene, benzene sulfonic acid, etc).
A nucleophilic aromatic substitution is a type of chemical reaction where an electron-rich nucleophile displaces a leaving group (for example, a halide on the aromatic ring). There are six types of nucleophilic substitution mechanisms: 1-the SNAr (addition-elimination) mechanism, whose name is due to the Hughes-Ingold symbol ''SN' and a unimolecular mechanism; 2-the SN1 reaction that produces diazonium salts 3-the benzyne mechanism that produce highly reactive species (including benzyne) derived from the aromatic ring by the replacement of two substituents; 4-the free radical SRN1 mechanism where a substituent on the aromatic ring is displaced by a nucleophile with the formation of intermediary free radical species; 5-the ANRORC (Addition of the Nucleophile, Ring Opening, and Ring Closure) mechanism, involved in reactions of metal amide nucleophiles and substituted pyrimidines; and 6-the Vicarious nucleophilic substitution, where a nucleophile displaces an H atom on the aromatic ring but without leaving groups (such as, for example, halogen substituents).
Ferromagnesian silicate minerals (i looked it up)
We know that the molar mass of N is 14 and O is 16,
therefore the molar mass of N2O is:
molar mass N2O = 14 * 2 + 16 = 44 g/mol
The number of moles:
moles N2O = 0.187 / 44
moles N2O = 0.00425 mol
There are 2 moles of N per 1 mole of N2O hence:
moles N = 0.00425mol * 2
<span>moles N = 0.0085 mol</span>
Answer : The partial pressure of
and
are, 84 torr and 778 torr respectively.
Explanation : Given,
Mass of
= 15.0 g
Mass of
= 22.6 g
Molar mass of
= 197.4 g/mole
Molar mass of
= 32 g/mole
First we have to calculate the moles of
and
.

and,

Now we have to calculate the mole fraction of
and
.

and,

Now we have to partial pressure of
and
.
According to the Raoult's law,

where,
= partial pressure of gas
= total pressure of gas
= mole fraction of gas


and,


Therefore, the partial pressure of
and
are, 84 torr and 778 torr respectively.
Answer:
It exerts a pressure of 3.6 atm
Explanation:
This is a gas law problem. We are looking at volume and pressure with temperature being kept constant, thus, the gas law to use is Boyle’s law. It states that at a given constant temperature, the volume of a given mass of gas is inversely proportional to the pressure of the gas.
Mathematically; P1V1 = P2V2
Let’s identify the parameters according to the question.
P1 = 1.2 atm
V1 = 375mL
P2 = ?
v2 = 125mL
We arrange the equation to make room for P2 and this can be written as:
P2 = P1V1/V2
P2 = (1.2 * 375)/125
P2 = 3.6 atm