Answer : The partial pressure of 
at equilibrium is, 1.0 × 10⁻⁶
Explanation :
The partial pressure of 
= 
The partial pressure of = 
The partial pressure of 
=
The balanced equilibrium reaction is,
Initial pressure 1.0×10⁻² 2.0×10⁻⁴ 2.0×10⁻⁴
At eqm. (1.0×10⁻²-2p) (2.0×10⁻⁴+p) (2.0×10⁻⁴+p)
The expression of equilibrium constant 
for the reaction will be:
Now put all the values in this expression, we get :
The partial pressure of at equilibrium = (2.0×10⁻⁴+(-1.99×10⁻⁴) )= 1.0 × 10⁻⁶
Therefore, the partial pressure of at equilibrium is, 1.0 × 10⁻⁶
Answer:
domain bacteria
Explanation:
Salmonella and E. coli are same in the sense that they are both bacteria,
Answer:
conduction
Explanation:
Conduction is the transfer of heat between substances that are in direct contact with each other. ... Conduction occurs when a substance is heated, particles will gain more energy, and vibrate more. These molecules then bump into nearby particles and transfer some of their energy to them.
The answer is c. because you have to increase concentration of h2
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).
