<span>(19.55 mol Au) / ( 1 ) x (196.97 g Au) / ( 1 mol Au) =
19.55 x 196.97 =
3850.76 g Au
I hope this helps you and have a great day!! :)
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Answer : The volume of the cube submerged in the liquid is, 29.8 mL
Explanation :
First we have to determine the mass of ice.
Formula used :
Given:
Density of ice = 
Volume of ice = 45.0 mL
The cube will float when 40.5 g of liquid is displaced.
Now we have to determine the volume of the cube is submerged in the liquid.
Thus, the volume of the cube submerged in the liquid is, 29.8 mL
Answer:
The equation for the rate of this reaction is R = [NO] + {O2}
Explanation:
The rate-determining step of a reaction is the slowest step of a chemical reaction which determines the rate (speed) at which the overall reaction would take place.
Reaction mechanism:
The slow and fast reactions both have NO3 which is cancelled out on both sides, in order to get the overall reaction.
The rate law for this reaction would be that for the rate determining step:
R = [NO] + {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).
