Answer:
Approximately 0.36 grams, because copper (II) chloride acts as a limiting reactant.
Explanation:
- It is a stichiometry problem.
- We should write the balance equation of the mentioned chemical reaction:
<em>2Al + 3CuCl₂ → 3Cu + 2AlCl₃.</em>
- It is clear that 2.0 moles of Al foil reacts with 3.0 moles of CuCl₂ to produce 3.0 moles of Cu metal and 2.0 moles of AlCl₃.
- Also, we need to calculate the number of moles of the reported masses of Al foil (0.50 g) and CuCl₂ (0.75 g) using the relation:
<em>n = mass / molar mass</em>
- The no. of moles of Al foil = mass / atomic mass = (0.50 g) / (26.98 g/mol) = 0.0185 mol.
- The no. of moles of CuCl₂ = mass / molar mass = (0.75 g) / (134.45 g/mol) = 5.578 x 10⁻³ mol.
- <em>From the stichiometry Al foil reacts with CuCl₂ with a ratio of 2:3.</em>
∴ 3.85 x 10⁻³ mol of Al foil reacts completely with 5.578 x 10⁻³ mol of CuCl₂ with <em>(2:3)</em> ratio and CuCl₂ is the limiting reactant while Al foil is in excess.
- From the stichiometry 3.0 moles of CuCl₂ will produce the same no. of moles of copper metal (3.0 moles).
- So, this reaction will produce 5.578 x 10⁻³ mol of copper metal.
- Finally, we can calculate the mass of copper produced using:
mass of Cu = no. of moles x Atomic mass of Cu = (5.578 x 10⁻³ mol)(63.546 g/mol) = 0.354459 g ≅ 0.36 g.
- <u><em>So, the answer is:</em></u>
<em>Approximately 0.36 grams, because copper (II) chloride acts as a limiting reactant.</em>
Answer:
S°m,298K = 85.184 J/Kmol
Explanation:
∴ T = 10 K ⇒ Cp,m(Hg(s)) = 4.64 J/Kmol
∴ 10 K to 234.3 K ⇒ ΔS = 57.74 J/Kmol
∴ T = 234.3 K ⇒ ΔHf = 2322 J/mol
∴ 234.3 K to 298.0 K ⇒ ΔS = 6.85 J/Kmol
⇒ S°m,298K = S°m,0K + ∫CpdT/T(10K) + ΔS(10-234.3) + ΔHf/T(234.3K) + ΔS(234.3-298)
⇒ S°m,298K = 0 + 10.684 J/Kmol + 57.74 J/Kmol + 9.9104 J/Kmol + 6.85 J/kmol
⇒ S°m,298K = 85.184 J/Kmol
Answer:
Diet: fruit, leaves, bark, stems, seeds, eggs, insects, birds, small to medium sized primates - red tail monkeys, yellow baboons, bushbuck and warthogs.
Environmental Relationship - The chimpanzee keeps the plants it eats short, moves dirt around which helps things living in the dirt, keeps bird and small monkey populations that it eats from overpopulating.
Different biotic and abiotic factors affect why the chimps live where they do. (Spatial Relationships)
Explanation:
Answer: 0.67 moles of 
Explanation:
According to avogadro's law, 1 mole of every substance occupies 22.4 L at STP and contains avogadro's number 
of particles.
To calculate the moles, we use the equation:
According to stoichiometry:
3 moles of 
is produced by 2 moles of
Thus 1 mole of is produced by= 
of
Thus 0.67 moles of are required to produce 28.3 g of
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).
