Answer: 8556 mm, or 855.6 cm (8560 mm to 3 sig figs)
Explanation: Convert mm to cm by dividing by 10 (1cm/10mm)
Find the area of the foil face in cm^2 (30cm*0.2020cm) = 0.606 cm^2
Calculate the volume occupied by 1.40 kg of foil in cm^3. 1.40kg = 1400g
1.400g/(2.7 g/cm^3) = 518.5 cm^3 for 1.40 kg Au
Volume = Area (of the face) * Length
We want Length:
Length = Volume/Area
L = (518.5 cm^3/0.606 cm^2)
L = 855.6 cm (8556 mm) Round to 3 sig figs (856 cm and 8560 mm)
Explanation:
6 F2------->4 AlF3
F2-----------> 4/6 AlF3
8.25 F2 ---------> 4×8.25/6 AlF3
so 5.5 moles
Answer:
1) The value of Kc:
C. remains the same.
2) The value of Qc:
A. is greater than Kc.
3) The reaction must:
B. run in the reverse direction to restablish equilibrium.
4) The concentration of N2 will:
B. decrease.
Explanation:
Hello,
In this case, by means of the Le Chatelier's principle which is based on the shift a chemical reaction could have under some modifications, we have:
1) The value of Kc:
C. remains the same, since it just depend the reaction's thermodynamics as it is computed via:

2) The value of Qc:
A. is greater than Kc, since the reaction quotient is:
![Qc=\frac{[N_2][H_2]^3}{[NH_3]^2}](https://tex.z-dn.net/?f=Qc%3D%5Cfrac%7B%5BN_2%5D%5BH_2%5D%5E3%7D%7B%5BNH_3%5D%5E2%7D)
Thus, the lower the concentration of ammonia, the higher Qc, making Qc>Kc.
3) The reaction must:
B. run in the reverse direction to restablish equilibrium, since ammonia was withdrawn and should be regenerated to reach the equilibrium.
4) The concentration of N2 will:
B. decrease, since less reactant is forming the products.
Best regards.
A carboxylic acid is named in the IUPAC system by replacing the -e in the name of the parent alkane with -<u>oic acid</u>
<u></u>
<h3>What is carboxylic acid?</h3>
Carboxylic acid is an organic acid that contains a carboxyl group (C(=O)OH) attached to an R-group. The general formula of a carboxylic acid is R−COOH or R−CO2H, with R referring to the alkyl, alkenyl, aryl, or other group. Carboxylic acids occur widely. Important examples include the amino acids and fatty acids. Deprotonation of a carboxylic acid gives a carboxylate anion.
Carboxylic acids are commonly identified by their trivial names. They often have the suffix -ic acid. IUPAC-recommended names also exist; in this system, carboxylic acids have an -oic acid suffix. For example, butyric acid (C3H7CO2H) is butanoic acid by IUPAC guidelines. For nomenclature of complex molecules containing a carboxylic acid, the carboxyl can be considered position one of the parent chain even if there are other substituents, such as 3-chloropropanoic acid. Alternately, it can be named as a "carboxy" or "carboxylic acid" substituent on another parent structure, such as 2-carboxyfuran.
Learn more about carboxylic acid
brainly.com/question/26855500
#SPJ4