(a)
Interpretation:
The formulas for ammonium and ammonia are to be determined.
Concept introduction:
Covalent bonds are formed by the sharing of electrons between two or more atoms. In covalent bonding, there is a mutual attraction between two nuclei and the two electrons that reside between them. The elements that engage in covalent bond formation are present at the rightmost corner of the periodic table. These elements are non-metals. The interaction between two non-metal elements leads to the formation of a covalent bond.
(b)
Interpretation:
The formulas for magnesium sulfide, magnesium sulfite, and magnesium sulfate are to be determined.
Concept introduction:
The general rules for naming ionic compounds are as follows:
1) In ionic compounds, the cations are named before the anions.
2) In binary ionic compounds, the name of the cation is the same as the name of the metal. The name of the anion includes the root name of the non-metal and a suffix
3) In polyatomic ions in which a non-metal is bonded to one or more oxygen atoms. In two oxoanions in the family, the ion with fewer oxygen atoms has the non-metal root name and a suffix
(c)
Interpretation:
The formulas for hydrochloric acid, chloric acid, and chlorous acid are to be determined.
Concept introduction:
The general formula for naming binary acids is,
The general rules for naming the members of a family with four oxoanions are as follows:
1) The anion with the most number of oxygen atoms has the refix
2) The anion with one fewer oxygen atom has the non-metal root and the suffix
3) The anion with two fewer oxygen atoms has the non-metal root and the suffix
4) The anion with three fewer oxygen atoms has the prefix
(d)
Interpretation:
The formulas for cuprous bromide and cupric bromide are to be determined.
Concept introduction:
The general rules for naming ionic compounds with different charges on the same metal are:
1) The root name of the metal is followed by the suffix
2)The root name of the metal is followed by the suffix

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Chapter 2 Solutions
CHEMISTRY:MOLECULAR...V.2 W/ACCESS
- + C8H16O2 (Fatty acid) + 11 02 → 8 CO2 a. Which of the above are the reactants? b. Which of the above are the products? H2o CO₂ c. Which reactant is the electron donor? Futty acid d. Which reactant is the electron acceptor? e. Which of the product is now reduced? f. Which of the products is now oxidized? 02 #20 102 8 H₂O g. Where was the carbon initially in this chemical reaction and where is it now that it is finished? 2 h. Where were the electrons initially in this chemical reaction and where is it now that it is finished?arrow_forward→ Acetyl-CoA + 3NAD+ + 1FAD + 1ADP 2CO2 + CoA + 3NADH + 1FADH2 + 1ATP a. Which of the above are the reactants? b. Which of the above are the products? c. Which reactant is the electron donor? d. Which reactants are the electron acceptors? e. Which of the products are now reduced? f. Which product is now oxidized? g. Which process was used to produce the ATP? h. Where was the energy initially in this chemical reaction and where is it now that it is finished? i. Where was the carbon initially in this chemical reaction and where is it now that it is finished? j. Where were the electrons initially in this chemical reaction and where is it now that it is finished?arrow_forwardRank each of the following substituted benzene molecules in order of which will react fastest (1) to slowest (4) by electrophilic aromatic substitution. OCH 3 (Choose one) OH (Choose one) Br (Choose one) Explanation Check NO2 (Choose one) © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Aarrow_forward
- For each of the substituted benzene molecules below, determine the inductive and resonance effects the substituent will have on the benzene ring, as well as the overall electron-density of the ring compared to unsubstituted benzene. Molecule Inductive Effects O donating O withdrawing O no inductive effects Resonance Effects Overall Electron-Density ○ donating ○ withdrawing O no resonance effects O electron-rich O electron-deficient O similar to benzene Cl O donating O withdrawing ○ donating ○ withdrawing O no inductive effects O no resonance effects O Explanation Check O electron-rich O electron-deficient similar to benzene X © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Accessarrow_forwardIdentifying electron-donating and For each of the substituted benzene molecules below, determine the inductive and resonance effects the substituent will have on the benzene ring, as well as the overall electron-density of the ring compared to unsubstituted benzene. Molecule Inductive Effects NH2 ○ donating NO2 Explanation Check withdrawing no inductive effects Resonance Effects Overall Electron-Density ○ donating O withdrawing O no resonance effects O donating O withdrawing O donating withdrawing O no inductive effects Ono resonance effects O electron-rich electron-deficient O similar to benzene O electron-rich O electron-deficient O similar to benzene olo 18 Ar 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Accessibilityarrow_forwardRank each of the following substituted benzene molecules in order of which will react fastest (1) to slowest (4) by electrophilic aromatic substitution. Explanation Check Х (Choose one) OH (Choose one) OCH3 (Choose one) OH (Choose one) © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Centerarrow_forward
- Assign R or S to all the chiral centers in each compound drawn below porat bg 9 Br Brarrow_forwarddescrive the energy levels of an atom and howan electron moces between themarrow_forwardRank each set of substituents using the Cahn-Ingold-Perlog sequence rules (priority) by numbering the highest priority substituent 1.arrow_forward
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