(a)
Interpretation: The Lewis dot structure of the atoms has to be found by using their valence electrons present in the outermost shell.
Concept introduction: Lewis dot structures are also called electron dot structures. The diagrams are named after Gilbert N. Lewis, who described them in his 1916 article entitled The Atom and the Molecule.
A nucleus of an atom consists of neutrons and protons. Electrons are from closest to outermost shells around the nucleus. Proton and electron have +1 and -1 charge respectively. Neutron has no charge.
Number of protons is equal to number of electrons in the case of neutral atoms.
The number of electrons present in the outermost shell of an atom that participate in forming
Each group present in the periodic table has specific common valence electrons. Therefore, the position of the atom in the periodic table should be known for drawing the Lewis dot structures.
To find: Draw the Lewis dot structure of a boron atom
(b)
Interpretation: The Lewis dot structure of the atoms has to be found by using their valence electrons present in the outermost shell.
Concept introduction: Lewis dot structures are also called electron dot structures. The diagrams are named after Gilbert N. Lewis, who described them in his 1916 article entitled The Atom and the Molecule.
A nucleus of an atom consists of neutrons and protons. Electrons are from closest to outermost shells around the nucleus. Proton and electron have +1 and -1 charge respectively. Neutron has no charge.
Number of protons is equal to number of electrons in the case of neutral atoms.
The number of electrons present in the outermost shell of an atom that participate in forming chemical bonds with other atoms is called valence electrons.
Each group present in the periodic table has specific common valence electrons. Therefore, the position of the atom in the periodic table should be known for drawing the Lewis dot structures.
To find: Draw the Lewis dot structure of a nitrogen atom
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Chapter 1 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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