General Chemistry: Atoms First
2nd Edition
ISBN: 9780321809261
Author: John E. McMurry, Robert C. Fay
Publisher: Prentice Hall
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Chapter 4.9, Problem 4.18P
Interpretation Introduction
Interpretation:
Resonance structure of Nitrous oxide
Concept introduction:
Resonance hybrid:
Sum of valid electron dot structure of a molecule is called resonance hybrid. It shows overall delocalization of electrons within the molecule.
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[C‒H: 413; C‒C: 347; C=O: 745; C=C: 614; Cl‒Cl: 239, C‒O: 358; O‒H: 467]
Chapter 4 Solutions
General Chemistry: Atoms First
Ch. 4.2 - Prob. 4.1PCh. 4.2 - Prob. 4.2PCh. 4.2 - Prob. 4.3CPCh. 4.4 - Use the electronegativity values in Figure 4.4 to...Ch. 4.4 - Order the following compounds according to the...Ch. 4.4 - An electrostatic potential map of water is shown...Ch. 4.5 - Prob. 4.7PCh. 4.5 - Write formulas for compounds with the following...Ch. 4.5 - Prob. 4.9CPCh. 4.6 - Draw electron-dot structures for the following...
Ch. 4.6 - Draw an electron-dot structure for the hydronium...Ch. 4.7 - Draw electron-dot structures for the following...Ch. 4.7 - There are two molecules with the formula C2H6O....Ch. 4.7 - The following structure is a representation of...Ch. 4.8 - Carbon monoxide, CO, is a deadly gas produced by...Ch. 4.8 - Draw an electron-dot structure for each of the...Ch. 4.8 - Prob. 4.17PCh. 4.9 - Prob. 4.18PCh. 4.9 - Draw as many resonance structures as possible for...Ch. 4.9 - The following structure shows the connections...Ch. 4.10 - Calculate the formal charge on each atom in the...Ch. 4.10 - Calculate the formal charge on each atom in the...Ch. 4.10 - What is a radical, and why are they so reactive?Ch. 4.10 - Prob. 4.24PCh. 4.10 - Draw an electron-dot structure for the ethyl...Ch. 4 - Two electrostatic potential maps are shown, one of...Ch. 4 - Prob. 4.27CPCh. 4 - Prob. 4.28CPCh. 4 - Prob. 4.29CPCh. 4 - Sinapaldehyde, a compound present in the toasted...Ch. 4 - Vitamin C (ascorbic acid) has the following...Ch. 4 - What general trends in electronegativity occur in...Ch. 4 - Prob. 4.33SPCh. 4 - Prob. 4.34SPCh. 4 - Prob. 4.35SPCh. 4 - Prob. 4.36SPCh. 4 - Prob. 4.37SPCh. 4 - Prob. 4.38SPCh. 4 - Show the direction of polarity for each of the...Ch. 4 - Prob. 4.40SPCh. 4 - Prob. 4.41SPCh. 4 - Prob. 4.42SPCh. 4 - Prob. 4.43SPCh. 4 - Prob. 4.44SPCh. 4 - Prob. 4.45SPCh. 4 - Prob. 4.46SPCh. 4 - Prob. 4.47SPCh. 4 - Prob. 4.48SPCh. 4 - Prob. 4.49SPCh. 4 - Prob. 4.50SPCh. 4 - Which of the following substances contains an atom...Ch. 4 - Draw electron-dot structures for the following...Ch. 4 - Prob. 4.53SPCh. 4 - Oxalic acid, H2C2O4, is a mildly poisonous...Ch. 4 - Draw an electron-dot structure for carbon...Ch. 4 - Prob. 4.56SPCh. 4 - Prob. 4.57SPCh. 4 - Prob. 4.58SPCh. 4 - Prob. 4.59SPCh. 4 - Methylphenidate (C14H19NO2), marketed as Ritalin,...Ch. 4 - Pregabalin (C8H17NO2), marketed as Lyrica, is an...Ch. 4 - Draw as many resonance structures as you can that...Ch. 4 - Prob. 4.63SPCh. 4 - Which of the following pairs of structures...Ch. 4 - Which of the following pairs of structures...Ch. 4 - Draw an electron-dot structure for carbon...Ch. 4 - Prob. 4.67SPCh. 4 - Prob. 4.68SPCh. 4 - Prob. 4.69SPCh. 4 - Prob. 4.70SPCh. 4 - Prob. 4.71SPCh. 4 - Prob. 4.72SPCh. 4 - Prob. 4.73SPCh. 4 - Prob. 4.74CHPCh. 4 - Thiofulminic acid, , is a highly reactive...Ch. 4 - Draw two resonance structures for methyl...Ch. 4 - Prob. 4.78CHPCh. 4 - Prob. 4.79CHPCh. 4 - Prob. 4.80CHPCh. 4 - Prob. 4.81CHPCh. 4 - Prob. 4.82CHPCh. 4 - Prob. 4.83CHPCh. 4 - Prob. 4.84CHPCh. 4 - Prob. 4.85CHPCh. 4 - Sulfur reacts with chlorine to give a product that...Ch. 4 - Sulfur reacts with ammonia to give a product A...Ch. 4 - Prob. 4.88MPCh. 4 - Prob. 4.89MP
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- Draw all resonance structures for the nitric acid molecule, HNO3 (NO2OH).arrow_forwardChloral, Cl3C—CH=O, reacts with water to form the sedative and hypnotic agent chloral hydrate, Cl3C—CH(OH)2. Draw Lewis structures for these substances, and describe the change in molecular shape, if any, that occurs around each of the carbon atoms during the reaction.arrow_forwardWhich atom in the O-C single bond has a partial positive charge (δ⁺)?arrow_forward
- Calculate the enthalpy change for the following reactions using the bond enthalpy given below. (Bond enthalpy/kJ : H−H = 436, C−H = 413, C=O = 799, O=O = 495, O−H = 463) (a) H2(g) + 1⁄2O2(g) → H2O(g) (b) CH4(g) + 2O2(g) → CO2(g) + 2H2O(l)arrow_forwardCovalent bonds: H―HC―HO―HO═O C≡O Bond energy (kJ/mol):4364154654981080Calculate the enthalpy change (H, in kJ/mol) for the following reaction and indicate whether the reaction is exothermic or endothermic.(*BE for C═Oin CO2)(a) CH4(g)+ H2O(g)CO(g)+ 3H2(g);arrow_forwardThe two compounds nitrogen dioxide and dinitrogen tetraoxide are introduced in Section 3.13. (a) NO2 is an odd-electron compound. Draw the best Lewis diagrams possible for it, recognizing that one atom cannot achieve an octet configuration. Use formal charges to decide whether that should be the (central) nitrogen atom or one of the oxygen atoms. (b) Draw resonance forms for N2O4 that obey the octet rule. The two N atoms are bonded in this molecule.arrow_forward
- Using the bond energies provided, calculate the enthalpy of the reaction (∆Hrxn, in kJ) for the combustion of methanol shown below. CH3OH(l) +3/2 O2 (g) → CO2 (g) + 2 H2O(g)arrow_forwardDraw the two best Lewis dot resonance structures of OCN⁻ and explain which one is the better of the two and why.arrow_forwardAcetylene (C2H2) and nitrogen (N2) both contain a triplebond, but they differ greatly in their chemical properties.(a) Write the Lewis structures for the two substances. (b) By referring to Appendix C, look up the enthalpies of formationof acetylene and nitrogen. Which compound is more stable?(c) Write balanced chemical equations for the completeoxidation of N2 to form N2O5(g) and of acetylene to formCO2(g) and H2O(g). (d) Calculate the enthalpy of oxidationper mole for N2 and for C2H2 (the enthalpy of formationof N2O5(g) is 11.30 kJ/mol). (e) Both N2 and C2H2 possesstriple bonds with quite high bond enthalpies (Table 8.3).Calculate the enthalpy of hydrogenation per mole for bothcompounds: acetylene plus H2 to make methane, CH4;nitrogen plus H2 to make ammonia, NH3.arrow_forward
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