Chapter 9, Problem 9e
The molecule shown below is called furan. It is represented in typical shorthand way for organic molecules, with hydrogen atoms not shown, and each of the 4 vertices representing a carbon atom.
(e) The C¬C¬C bond angles in furan are much smaller than those in benzene. The likely reason is which of the following: (i) The hybridization of the carbon atoms in furan is different from that in benzene, (ii) Furan does not have another resonance structure equivalent to the one above, or (iii) The atoms in a five-membered ring are forced to adopt smaller angles than in a six-membered ring.
Video transcript
In the hydrocarbon
(d) Identify all the 120° bond angles in the molecule.
The drawing below shows the overlap of two hybrid orbitals to form a bond in a hydrocarbon. (a) Which of the following types of bonds is being formed: (i) C¬C s, (ii) C¬C p, or (iii) C¬H s?
The drawing below shows the overlap of two hybrid orbitals to form a bond in a hydrocarbon. (b) Which of the following could be the identity of the hydrocarbon: (i) CH4, (ii) C2H6, (iii) C2H4, or (iv) C2H2?
The following is part of a molecular orbital energy-level diagram for MOs constructed from 1s atomic orbitals.
(a) What labels do we use for the two MOs shown?
(a) An AB2 molecule is linear. How many nonbonding electron pairs are around the A atom from this information?
(b) How many nonbonding electrons surround the Xe in XeF2?