Concept explainers
(a)
Interpretation: The systematic name and common name of the given organic compound is to be interpreted.
Concept Introduction: Organic compounds are chemical compounds that are mainly composed of carbon and hydrogen atoms. The naming of organic compounds is followed the IUPAC rules. The longest chain of carbon atoms is considered the parent chain. The substituents must be given with the least locant number. The locant number must be written as the prefix in the IUPAC name.
(a)

Answer to Problem 47PP
The systematic name of the given compound must be 2-chloropropane and the common name is isopropyl chloride.
Explanation of Solution
In the given organic compound, the parent longest chain contains 3 carbon atoms so the root word must be propane with one substituent; chloro at C2 position. Thus, the systematic name of the given compound must be 2-chloropropane and the common name is isopropyl chloride.
(b)
Interpretation: The systematic name and common name of the given organic compound is to be interpreted.
Concept Introduction: Organic compounds are chemical compounds that are mainly composed of carbon and hydrogen atoms. The naming of organic compounds is followed the IUPAC rules. The longest chain of carbon atoms is considered the parent chain. The substituents must be given with the least locant number. The locant number must be written as the prefix in the IUPAC name.
(b)

Answer to Problem 47PP
The systematic name of the given compound must be 2-bromo-2-methylpropane and the common name is tert-butyl bromide.
Explanation of Solution
In the given organic compound, the parent longest chain contains 3 carbon atoms so the root word must be propane with two substituents: chloro and methyl at 2 positions. Thus, the systematic name of the given compound must be 2-bromo-2-methylpropane and the common name is tert-butyl bromide.
(c)
Interpretation: The systematic name and common name of the given organic compound is to be interpreted.
Concept Introduction: Organic compounds are chemical compounds that are mainly composed of carbon and hydrogen atoms. The naming of organic compounds is followed the IUPAC rules. The longest chain of carbon atoms is considered the parent chain. The substituents must be given with the least locant number. The locant number must be written as the prefix in the IUPAC name.
(c)

Answer to Problem 47PP
The systematic name of the given compound must be 1-iodopropane and the common name is propyl iodide.
Explanation of Solution
In the given organic compound the parent longest chain contains 3 carbon atoms so the root word must be propane with one substituent; iodo at 1 position. Thus, the systematic name of the given compound must be 1-iodopropane and the common name is propyl iodide.
(d)
Interpretation: The systematic name and common name of the given organic compound is to be interpreted.
Concept Introduction: Organic compounds are chemical compounds that are mainly composed of carbon and hydrogen atoms. The naming of organic compounds is followed the IUPAC rules. The longest chain of carbon atoms is considered the parent chain. The substituents must be given with the least locant number. The locant number must be written as the prefix in the IUPAC name.
(d)

Answer to Problem 47PP
The systematic name of the given compound must be (R)-2-bromobutane and the common name is (R)- sec-butyl bromide.
Explanation of Solution
In the given organic compound the parent longest chain contains 4 carbon atoms so the root word must be butane with one substituent; bromo at C2 position. Thus, the systematic name of the given compound must be (R)-2-bromobutane and the common name is (R)- sec-butyl bromide. The prefix (R) indicates the clockwise rotation of the groups bonded at the chiral C atom when arranged from 1 to 4 in the increasing order of their
(e)
Interpretation: The systematic name and common name of the given organic compound is to be interpreted.
Concept Introduction: Organic compounds are chemical compounds that are mainly composed of carbon and hydrogen atoms. The naming of organic compounds is followed the IUPAC rules. The longest chain of carbon atoms is considered the parent chain. The substituents must be given with the least locant number. The locant number must be written as the prefix in the IUPAC name.
(e)

Answer to Problem 47PP
The systematic name of the given compound must be 1-chloro-2,2- dimethylpropane and common name is neopentyl chloride.
Explanation of Solution
In the given organic compound, the parent longest chain contains 3 carbon atoms so the root word must be propane with three substituents as methyl and chloro at C1 and C2 position. Thus, the systematic name of the given compound must be 1-chloro-2,2- dimethylpropane and the common name is neopentyl chloride.
(f)
Interpretation: The systematic name and common name of the given organic compound is to be interpreted.
Concept Introduction: Organic compounds are chemical compounds that are mainly composed of carbon and hydrogen atoms. The naming of organic compounds is followed the IUPAC rules. The longest chain of carbon atoms is considered the parent chain. The substituents must be given with the least locant number. The locant number must be written as the prefix in the IUPAC name.
(f)

Answer to Problem 47PP
The systematic name of the given compound must be 4-bromo-3,3-dimethyl-4-propylhaptane.
Explanation of Solution
In the given organic compound the parent longest chain contains 7 carbon atoms so the root word must be haptane with four substituents as propyl, methyl and bromo. Thus, the systematic name of the given compound must be 4-bromo-3,3-dimethyl-4-propylhaptane.
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Chapter 7 Solutions
ORGANIC CHEMISTRY
- + 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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