Number 1 Bc of wood a magnetic
Answer
- continuous removal of PH3
- adding more of P into the system
Explanation:
In the reaction P4(g)+6H2(g) ⇌ 4PH3(g);
- The effect of temperature on equilibrium has to do with the heat of reaction. Recall that for an endothermic reaction, heat is absorbed in the reaction, and the value of ΔH is positive. Thus, for an endothermic reaction, we can picture heat as being a reactant:
heat+A⇌BΔH=+
- Since the reaction is endothermic reaction, heat is a absorbed. Decreasing the temperature will shift the equilibrium to the left, while increasing the temperature will shift the equilibrium to the right forming more of PH3.
- According to Le Chatelier’s principle, adding additional reactant to a system will shift the equilibrium to the right, towards the side of the products. In the same Way, reducing the concentration of the product will also shift equilibrium to the right continually forming PH3 as it is removed.
Answer:
Explanation:
Hermione is pretty smart. She realizes that, according to Dalton's Law of Partial Pressures, each gas exerts its pressure independently of the others, as if the others weren't even there.
She shows Ron how to use the Ideal Gas Law to solve the problem.
pV = nRT
She collects the data:
V = 1.00 L; n = 0.0319 mol; T = 25.0 °C
She reminds him to convert the temperature to kelvins
T = (25.0 +273.15) K = 298.15 K
Then she shows him how to do the calculation.
Isn't she smart?
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).
