Number 1 Bc of wood a magnetic
Answer is: volume of helium is 244.72 liters.
m(He) = 43.7 g.
n(He) = m(He) ÷ M(He).
n(He) = 43.7 g ÷ 4 g/mol.
n(He) = 10.925 mol.
V(He) = n(He) · n(He).
V(He) = 10.925 mol · 22.4 L/mol.
V(He) = 244.72 L.
Vm - molar volume at STP.
n - amount of substance.
Answer:
The value of the silver in the coin is 35.3 $
Explanation:
First of all, let's calculate the volume of the coin.
2π . r² . thickness = volume
r = diameter/2
r = 41 mm/2 = 20.5 mm
2 . π . (20.5 mm)² . 2.5 mm = 6601 mm³
Now, this is the volume of the coin, so we must find out how many grams are on it.
6601 mm³ / 1000 = 6.60 cm³
Let's apply density.
D = Mass / volume
10.5 g/cm³ = mass /6.60 cm³
10.5 g/cm³ . 6.60 cm³ = mass
69.3 g = mass
Each gram has a cost of 0.51$
69.3 g . 0.51$ = 35.3 $
Answer:
The structure can be found on the attached documents
Explanation:
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).