As one element .because po4 is phosphate for e.g.: NaPO4
The atomic number of an element never changes no matter how many neutrons they have so Sulfur would just have an atomic number of 16 like normal.
Answer:
Explanation:
We know we will need a balanced chemical equation with masses and molar masses, so, let's gather all the information in one place.
You don't tell us what the reaction is, but we can solve the problem so long as we balance the OH.
M_r: 58.32
Mg(OH)₂ + … ⟶ … + 2HOH
m/g: 58.3
(a) Moles of Mg(OH)₂
(b) Moles of H₂O
The molar ratio is 2 mol H₂O = 1 mol Mg(OH)₂.
The reaction will form 
of water.
<span>BaCl2+Na2SO4---->BaSO4+2NaCl
There is 1.0g of BaCl2 and 1.0g of Na2SO4, which is the limiting reagent?
"First convert grams into moles"
1.0g BaCl2 * (1 mol BaCl2 / 208.2g BaCl2) = 4.8 x 10^-3 mol BaCl2
1.0g Na2SO4 * (1 mol Na2SO4 / 142.04g Na2SO4) = 7.0 x 10^-3 mol Na2SO4
(7.0 x 10^-3 mol Na2SO4 / 4.8 x 10^-3 mol BaCl2 ) = 1.5 mol Na2SO4 / mol BaCl2
"From this ratio compare it to the equation, BaCl2+Na2SO4---->BaSO4+2NaCl"
The equation shows that for every mol of BaCl2 requires 1 mol of Na2SO4. But we found that there is 1.5 mol of Na2SO4 per mol of BaCl2. Therefore, BaCl2 is the limiting reagent.</span>
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).
