Answer:

Explanation:
From the question, we have been asked to find the molarity of FeCl2 having a volume of 450 mL,
We have been provided with 225 g which is proportional to 1.8 moles.
We know that molarity of any solution should be in mol/L.
1 mole contained in 1 L means it has a molarity of 1 mol/L
Let's convert 450 mL to Litres which is,

= 0.450 L
Thus,
1 mole is contained in 1L
x moles are contained in 0.450 L
Hence,
x mole/molarity = {1 mole x 1 L}/{0.450 L}
= 4 mol/L
Therefore 4 mol/L is the molar concentration.
Answer:
Explanation:
The absorbed sunlight drives photosynthesis, fuels evaporation, melts snow and ice, and warms the Earth system. Solar power drives Earth's climate. Energy from the Sun heats the surface, warms the atmosphere, and powers the ocean currents.
Answer:
Work is the use of force to move an object. It is directly related to both the force applied to the object and the distance the object moves. Work can be calculated with this equation: Work = Force x Distance.
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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).
dilution
V₁M₁=V₂M₂
V₁.12 = 100.6
V₁=50 ml
Add water 50 ml to 50 ml 12 M