Consider the reaction BF3 + NH3 -> F3B-NH3 (a) Describe the changes in hybridization of the B and N atoms as a result of this reaction. (b) Describe the shapes of all the reactant molecules with their bond angles. (c) Draw the overall shape of the product molecule and identify the bond angles around B and N atoms. (d) What is the name of the bond between B and N. (e)Describe the bonding orbitals that make the B and F, B and N & N and H bonds in the product molecule.

Consider the reaction BF3 + NH3 -> F3B-NH3 (a) Describe the changes in hybridization of the B and N atoms as a result of this reaction. (b) Describe the shapes of all the reactant molecules with their bond angles. (c) Draw the overall shape of the product molecule and identify the bond angles around B and N atoms. (d) What is the name of the bond between B and N. (e)Describe the bonding orbitals that make the B and F, B and N & N and H bonds in the product molecule.

Chemistry: Principles and Practice

3rd Edition

ISBN:9780534420123

Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward Mercer

Publisher:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward Mercer

Chapter9: Chemical Bonds

Section: Chapter Questions

Problem 9.72QE: Write all resonance structures of chlorobenzene, C6H5Cl, a molecule with the same cyclic structure...

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Given the bonds C N, C H, C Br, and S O, (a) which atom in each is the more electronegative? (b) which of these bonds is the most polar?
Write all resonance structures of chlorobenzene, C6H5Cl, a molecule with the same cyclic structure as benzene. In all structures, keep the CCl bond as a single bond. Which resonance structures are the most important?
The structural formulas for ethanol, CH3CH2OH, and propene, CH;CH=CH,2, are нн H Н—С—С—0—н H-C-C=C-H нн H H H Ethanol Propene (a) Complete the Lewis structure for each molecule showing all valence electrons. (b) Using the VSEPR model, predict all bond angles in each molecule.
Identify the set of covalent bonds that shows the correct trend of increasing bond polarity. (A) H―F < H―Cl < H―Br < H―I; (B) H―C < H―N < H―O < H―F; (C) H―O < H―S < H―Se < H―Te; (D) H―C < H―Si < H―Ge < H―Sn;
Consider the collection of nonmetallic elements O, P, Te,I, and B. (a) Which two would form the most polar singlebond? (b) Which two would form the longest single bond?(c) Which two would be likely to form a compound of formulaXY2? (d) Which combinations of elements would likelyyield a compound of empirical formula X2Y3?
19. :O: || :0-N- O: Which of the following statements, if true, would support the claim that the NO3 ion, represented above, has three resonance structures? (A) The NO3 ion is not a polar species. (B) The oxygen-to-nitrogen-to-oxygen bond angles are 90°. (C) One of the bonds in NO3 is longer than the other two. (D) One of the bonds in NO3¯ is shorter than the other two.
Hydrazine, N₂H₄, and carbon disulfide, CS₂, form a cyclicmolecule(right).(a) Draw Lewisstructures for N₂H₄ and CS₂. (b) How do electron-group arrange-ment, molecular shape, and hy-bridization of N change when N₂H₄ reacts to form the product?(c) How do electron-group arrangement, molecular shape, andhybridization of C change when CS₂ reacts to form the product?
Which of the following bonds are polar: (a) P—O; (b) S—F; (c) Br—Br; (d) O—Cl? Which is the more electronegative atom in each polar bond?
(a) Describe the molecule xenon trioxide, XeO3, using four possible Lewis structures, one each with zero, one, two, or three Xe—O double bonds. (b) Do any of these resonance structures satisfy the octet rule for every atom in the molecule? (c) Do any of the four Lewis structures have multiple resonance structures? If so, how many resonance structures do you find? (d) Which of the Lewis structures in (a) yields the most favorable formal charges for the molecule?
Write Lewis structures for the following: (c) C2F6 (contains a C¬C bond), (d) AsO3 3 -, (e) H2SO3 (H is bonded to O), (f) NH2Cl.. Arrange the bonds in each of the following sets in order of increasing polarity: (a) C¬F, O¬F, Be¬F; (b) O¬Cl, S¬Br, C¬P; (c) C¬S, B¬F, N¬O. What is the Lewis symbol for each of the following atoms or ions? (a) K, (b) As, (c) Sn2 + , (d) N3 Write electron configurations for the following ions and determine which have noble-gas configurations: (a) Cd2+, (b) P3-, (c) Zr4+
An elemental analysis of a hydrocarbon, which contains only carbon and hydrogen, shows the mass%: element mass% carbon 92.26 hydrogen 7.743 (A) * Determine the empirical formula of the hydrocarbon. (B) The compound has a molar mass of 26.04 g/mol. Determine its molecular formula. (C, Draw the Lewis structure of the molecular compound. Count the total number of sigma bonds and pi bonds each, present in the molecule. (D, What is the hybridization of carbon in the molecule? Explain.
Acetylene (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.