The excess reactant is Aluminum.
<u>Explanation:</u>
We have to write the balanced equation as,
4 Al+ 3 O₂ → 2 Al₂O₃
According to the molar ratio 4: 3, from the given balanced equation, we can say that 4 atoms of Al reacted with 3 molecules of oxygen.
Given that 10 atoms of aluminum reacts with 6 molecules of oxygen, as per the ratio only 8 atoms of Aluminum is required to react with 6 molecules of oxygen, so excess reactant is Aluminum.
Answer:
ΔS surrounding (entropy change of the reservoir) = -1 J/K
Explanation:
Given:
Change in heat (ΔH) = 150 joules
Temperature (T) = 150 K
Find:
ΔS surrounding (entropy change of the reservoir)
Computation:
ΔS surrounding (entropy change of the reservoir) = - ΔH / T
ΔS surrounding (entropy change of the reservoir) = - 150 / 150
ΔS surrounding (entropy change of the reservoir) = -1 J/K
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).
Answer:
1,2 and 4 are correct
Explanation:
Enzymes that show cooperativity are defined as Allosteric enzymes. This cooperativity is of several types.
1) homotropic/homoallestery - positive cooperation
2) heterotropic/heteroallestery - negative cooperation
Activity of allosteric enzymes is regulated by other molecules (effector molecules)
Hence, statement 1 and 2 are correct.
Binding curve of allosteric enzymes:
For cooperative binding, binding curve is Sigmoidal curve
For non cooperative binding, binding curve is Hyperboilc curve.
Hence, statement 3 is wrong.
Allosteric enzymes have multiple active sites.
Allosteric enzymes are often multi sub unit proteins.
Hence, statement 4 is correct.
