Concept explainers
(a)
Interpretation:
Compound
Concept Introduction:
Ionic compounds are named considering the cation and anion present in it. The cation part is written first followed by the anion part.
Rules for naming ionic compounds:
- The cation and anion present in the ionic compound has to be identified. Oxidation number of the cation has to be decided in order to cancel the charge of the negative anions.
- Cation is named first. In case, if the metal belongs to
transition metals , then the oxidation number is shown using Roman numeral and entered in parenthesis. - Anion has to be named next. If monoatomic anion is present, then the element name is ended with –ide. If an oxoanion is present then suffix –ate is added for the ion that has large number of oxygen atoms and suffix –ite is added for the ion that has less number of oxygen atoms. If the element can form a series of four oxoanions, then for the oxoanion having the less number of oxygen atoms, prefix hypo- is added and prefix per- is added if the oxoanion contains highest number of oxygen atoms.
- If water molecule is present in the formula of the ionic compound, then the word hydrate is added along with the Greek prefix that correspond to the number of water molecules present in it.
(b)
Interpretation:
Compound
Concept Introduction:
Refer part (a).
(c)
Interpretation:
Compound
Concept Introduction:
Refer part (a).
(d)
Interpretation:
Compound
Concept Introduction:
Binary molecular compounds are named by using the elements present in it and the number of atoms present in a molecule.
Rules for naming molecular compounds:
- First element name is written as such that is followed by the name of the second element in which the suffix is changed to –ide.
- Greek prefixes are used to indicate the number of atoms of each element that is present. Generally prefix mono- is ignored.
(e)
Interpretation:
Compound
Concept Introduction:
Refer part (a).
(f)
Interpretation:
Compound
Concept Introduction:
Refer part (a).
(g)
Interpretation:
Compound
Concept Introduction:
Refer part (a).
(h)
Interpretation:
Compound
Concept Introduction:
Refer part (a).
(i)
Interpretation:
Compound
Concept Introduction:
Refer part (a).

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Chapter F Solutions
ACHIEVE/CHEMICAL PRINCIPLES ACCESS 2TERM
- + 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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