A 3D representation of a cyclohexane (C,H12) molecule, a cyclic compound used in the manufacture of nylon and found in the distillation ofpetroleum, is shown. What is the molecular geometry around each carbon atom? molecular geometry:
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- Ketene, C2H2O, is a reactant for synthesizing cellulose acetate, which is used to make films, fibers, and fashionable clothing. (a) Write the Lewis structure of ketene. Ketene does not contain an OH bond. (b) Identify the electron-region geometry and the molecular geometry around each carbon atom and all the bond angles in the molecule. (c) Identify the hybridization of each carbon and oxygen atom. (d) Is the molecule polar or nonpolar? Use appropriate data to support your answer.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.indicate the approximate values for the indicated bond angles in the following molecules. 1 (a) H 0-N=ö 2. Н 4 H. (b) H C-c=0 H H H (c) H-N-O–H . H. (d) H-C-C=N: H.
- In the following compounds, the C atoms form a single ring.Draw a Lewis structure for each compound, identify cases for which resonance exists, and determine the carbon-carbon bondorder(s): (a) C₃H₄; (b) C₃H₆; (c) C₄H₆; (d) C₄H₄; (e) C₆H₆.Specify the local electron geometries about the atoms labelled a-d. Unshared electron pairs affect local geometry and are included in the structural formula. For each atom enter one of the following: tetrahedral, square planar, trigonal planar, trigonal pyramidal, or linear. (a) (b) (c) (d) H- H H-C H H H H H 05 > -HWhich of the following can be used to explain why all bond distances and angles in methane, CH4, are the same? (a) resonance; (b) delocalization of elec tron s; (c) bond polarities; (d) electron ega tivity; (e) orbit al hybridization.
- Tetrachloroethylene, C2Cl4, is used commercially as a dry-cleaning solvent. Propose a structure for tetrachloroethene based on the common bonding patterns expected in organic molecules. What kind of carbon–carbon bond ispresent?Formula Lewis Electron Molecular Bond Polar or Attractive Structure Pair Geometry Angle Force Non Polar Geometry Between Molecules CH4 Around First C Around First C C2H4 Around First C Around First C C,H2 Around First C Around First C CH;OH Around O Around O C2H;OH Around O Around O CH20 CH,OCH, Around O Around O CH;COOH Central C Central C НСООН Central C Central C CH;NH2 Around N Around N CH;COCH; Central C Central C(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.
- The carbon–carbon bond length in C2H2 is 1.20 Å, that inC2H4 is 1.34 Å, and that in C2H6 is 1.53 Å. Near which ofthese values would you predict the bond length of C2 tolie? Is the experimentally observed value, 1.31 Å, consistent with your prediction?10. The following Lewis structures for (a) HCN, (b) C3H;, (c) SnOz, (d) BF3, (e)HOF are incorrect. Explain what is wrong with each one and give a correct structure for the molecule. (Relative positions of atoms are shown correctly.) (a) H-ëN (b) HCC-H (c) 0-Sn-0 (d) :F B :F: (e) H-O-F: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?