The link below is a picture of the "Waning gibbus" phase, really hope that it helps you out :D
3Mg + N₂ → Mg₃N₂
n(Mg) = 12,2g÷24,4g/mol = 0,5mol - limiting reagente.
n(N₂) = 5,16g÷28g/mol = 0,18mol
n(Mg₃N₂):n(Mg) = 1:3, n(Mg₃N₂) = 0,166mol
m(Mg₃N₂) = 0,166mol·101,2g/mol = 16,8g.
%(N)= 2·Ar(N)÷Mr(Mg₃N₂) = 2·14÷101,2 = 27,66% = 0,2766
%(Mg) = 3·Ar(Mg)÷Mr(Mg₃N₂) = 3·24,4÷101,2 = 72,34%
or 100% - 27,66% = 72,34%.
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).
Equation is as follow,
Fe₂O₃ + 3 CO → 2 Fe + 3 CO₂
Oxidation:
3 CO → 3 CO₂
Oxidation state of C in CO is +2, and that in CO₂ is +4. So, carbon has lost 2 electrons per mole and 6 electrons per 3 moles hence,
3 CO → 3 CO₂ + 6 e⁻
Reduction:
Fe₂O₃ → 2 Fe
Oxidation state of Fe in Fe₂O₃ is +3 per atom, and that in Fe is 0. So, Iron has gained 3 electrons per atom and 6 electrons per 2 atoms hence,
Fe₂O₃ + 6e⁻ → 2 Fe
Result:
Iron in Fe₂O₃ has been reduced in this reaction and has played a role of oxidizing agent by oxidizing carbon from +2 state to +4 state.
