(a) How does the structure of diborane (B2H6) differ fromthat of ethane (C2H6)? (b) Explain why diborane adoptsthe geometry that it does. (c) What is the significance ofthe statement that the hydrogen atoms in diborane aredescribed as “hydridic”?
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(a) How does the structure of diborane (B2H6) differ from
that of ethane (C2H6)? (b) Explain why diborane adopts
the geometry that it does. (c) What is the significance of
the statement that the hydrogen atoms in diborane are
described as “hydridic”?
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- A carbene is a compound that has a carbon bonded to twoatoms and a lone pair remaining on the carbon. Manycarbenes are very reactive. (a) Draw the Lewis structurefor the simplest carbene, H2C. (b) Predict the length of thecarbon–carbon bond you would expect if two H2C moleculesreacted with each other by a combination reaction.(a) Triazine, C3 H3 N3, is like benzene except that in triazineevery other C¬H group is replaced by a nitrogen atom.Draw the Lewis structure(s) for the triazine molecule. (b) Estimatethe carbon–nitrogen bond distances in the ring.(a) Triazine, C3 H3 N3, is like benzene except that in triazineevery other C¬H group is replaced by a nitrogen atom. Draw the Lewis structure(s) for the triazine molecule. (b) Estimatethe carbon–nitrogen bond distances in the ring.
- Propylene, C3H6, is a gas that is used to form the importantpolymer called polypropylene. Its Lewis structure is (a) What is the total number of valence electrons in the propylenemolecule? (b) How many valence electrons are usedto make s bonds in the molecule? (c) How many valenceelectrons are used to make p bonds in the molecule? (d) Howmany valence electrons remain in nonbonding pairs in themolecule? (e) What is the hybridization at each carbon atomin the molecule?Calculate the Enthalpy Change (ΔH) from average bond energies, which have been listed below in KJ/mol, for the following reaction and identify the nature of the reaction: CH3COOH + CH3OH → CH3COOCH3 + H2O [C‒H: 413; C‒C: 347; C=O: 745; C=C: 614; Cl‒Cl: 239, C‒O: 358; O‒H: 467]Acetylene 1C2H22 and nitrogen 1N22 both contain a triplebond, but they differ greatly in their chemical properties.(a) Write the Lewis structures for the two substances. (b) Byreferring 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 N2O51g2 and of acetylene to formCO21g2 and H2O1g2. (d) Calculate the enthalpy of oxidationper mole for N2 and for C2H2 (the enthalpy of formationof N2O51g2 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.
- (a) Construct a Lewis structure for O2 in which each atomachieves an octet of electrons. (b) How many bondingelectrons are in the structure? (c) Would you expect theO¬O bond in O2 to be shorter or longer than the O¬Obond in compounds that contain an O¬O single bond?Explain.Rubbing alcohol is the common name for 2-propanol (iso- propanol), C3H7OH. (a) Draw the three-dimensional structure of the 2-propanol molecule and predict the geometry around each carbon atom. (b) Is the 2-propanol molecule polar or nonpolar? (c) What kinds of intermolecular attractive forces exist between the 2-propanol molecules? (d) The isomer 1-propanol has the same molecular weight as 2-propanol, yet 2-propanol boils at 82.6 °C and 1-propanol boils at 97.2 °C. Explain the difference.Draw a Lewis structure for each of the following molecule: (a) chlorodifluoromethane, CHCIF2 (b) propanoic acid C2H5CO2H (basic structure pictured below) (c) acetonitrile, CH3CN ( the framework is H3C-C-N) (d) allene, H2CCCH2
- (a) Compare the bond enthalpies (Table 8.3) of the carbon–carbon single, double, and triple bonds to deduce an averageπ -bond contribution to the enthalpy. What fraction ofa single bond does this quantity represent? (b) Make a similarcomparison of nitrogen–nitrogen bonds. What do youobserve? (c) Write Lewis structures of N2H4, N2H2, and N2,and determine the hybridization around nitrogen in eachcase. (d) Propose a reason for the large difference in yourobservations of parts (a) and (b).State whether each of these statements is true or false. (a)A carbon–carbon triple bond is shorter than a carbon–carbonsingle bond. (b) There are exactly six bonding electrons inthe O2 molecule. (c) The C—O bond in carbon monoxide islonger than the C—O bond in carbon dioxide. (d) The O—Obond in ozone is shorter than the O—O bond in O2. (e) Themore electronegative the atom, the more bonds it makes toother atoms.2(a) Provide the Lewis structures for both CH3OH and C2H3Cl. 2(b) What is the largest bond angle among all the bond angles in CH3OH and C2H3Cl? Listthe three atoms making this largest bond angle, and estimate the value of the angle.2(c) What intermolecular forces are present(i) between CH3OH molecules?(ii) between C2H3Cl molecules?