Answer:
The concentration of Li (in wt%) is 3,47g/mol
Explanation:
To obtain the 2,42g/cm³ of density:
2,42g/cm³ = 2,71g/cm³X + 0,534g/cm³Y <em>(1)</em>
<em>Where X is molar fraction of Al and Y is molar fraction of Li.</em>
X + Y = 1 <em>(2)</em>
Replacing (2) in (1):
Y = 0,13
Thus, X = 0,87
The weight of Al and Li is:
0,87*26,98g/mol = 23,4726 g of aluminium
0,13*6,941g/mol = 0,84383 g of lithium
The concentration of Li (in wt%) is:
0,84383g/(0,84383g+23,4726g) ×100= <em>3,47%</em>
Maybe 24% not sure try researching it on google
Answer:
Molarity of NaOH = 1.8 M.
Explanation:
From the question given above, the following data were obtained:
Mass of NaOH = 36 g
Molar mass of NaOH = 40 g/mol
Volume = 500 mL
Molarity of NaOH =?
Next, we shall determine the number of mole in 36 g of NaOH. This can be obtained as follow:
Mass of NaOH = 36 g
Molar mass of NaOH = 40 g/mol
Mole of NaOH =?
Mole = mass / molar mass
Mole of NaOH = 36 / 40
Mole of NaOH = 0.9 mole
Next, we shall convert 500 mL to L. This can be obtained as follow:
1000 mL = 1 L
Therefore,
500 mL = 500 mL × 1 L / 1000 mL
500 mL = 0.5 L
Finally, we shall determine the molarity of NaOH. This can be obtained as follow:
Mole of NaOH = 0.9 mole
Volume = 0.5 L
Molarity of NaOH =?
Molarity = mole / Volume
Molarity of NaOH = 0.9 / 0.5
Molarity of NaOH = 1.8 M
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).