Answer: The concentrations of A , B , and C at equilibrium are 0.1583 M, 0.2583 M, and 0.1417 M.
Explanation:
The reaction equation is as follows.
Initial : 0.3 0.4 0
Change: -x -x x
Equilbm: (0.3 - x) (0.4 - x) x
We know that, relation between standard free energy and equilibrium constant is as follows.
Putting the given values into the above formula as follows.
x = 0.1417
Hence, at equilibrium
= 0.1583 M
= 0.2583 M
Answer:
mass/13of molecules .........
Answer:
The baseball is thrown twice as fast as the softball in the same direction.
Explanation:
Actually, we can answer the problem even without the first statement. All we have to do is write the reaction for the production of sulfur trioxide.
2 S + 3 O₂ → 2 SO₃
The stoichiometric calculations is as follows:
6 g S * 1 mol/32.06 g S = 0.187 mol S
Moles O₂ needed = 0.187 mol S * 3 mol O₂/2 mol S = 0.2805 mol O₂
Since the molar mas of O₂ is 32 g/mol,
Mass of O₂ needed = 0.2805 mol O₂ * 32 g/mol = 8.976 g O₂
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).
