Concept explainers
Ethylene oxide is an intermediate in the manufacture or ethylene glycol (antifreeze) and polyester
(a) What are the bond angles in the ring? Comment on the relation between the bond angles expected based on hybridization an d the bond angles expected for a three-member ring.
(b) Is the molecule polar? Based on the electrostatic poten1ial map shown below. where do the neg-alive and positive charges lie in the molecule?
Polarity: It is a well separation of electric charge leading to a molecule or chemical compounds having an electrical dipole moment. Generally the polar molecules must contain polar bonds due to a different in electronegative between the bonded atoms.
The electrostatic potential map clearly to explain, the oxygen atom has more negative (δ–) charge and other side has less positive (δ–) charge, so this molecule is a more polar nature.
Trending nowThis is a popular solution!
Chapter 9 Solutions
Chemistry & Chemical Reactivity
- H2CO molecules (a) use orbital hybridization theory to determine the molecular shape of h2co. (b) what bonds are formed between the c and o atoms in formaldehyde molecules?arrow_forwardBond energy : 4. (a) Draw the Lewis structure of NH,BCI, and name the bond between N and B. (b) State the type of orbital hybridization of N in NH3 and in NH3BCI3. NH3: NH;BCI3:arrow_forward(a) Methane (CH4) and the perchlorate ion (ClO4- ) are bothdescribed as tetrahedral. What does this indicate about theirbond angles? (b) The NH3 molecule is trigonal pyramidal, while BF3 is trigonal planar. Which of these molecules is flat?arrow_forward
- For each statement, indicate whether it is true or false. (a) The greater the orbital overlap in a bond, the weaker the bond. [b] The greater the orbital overlap in a bond, the shorter the bond. [c] To create a hybrid orbital, you could use the s orbital on one atom with a p orbital on another atom. [d] Nonbonding electron pairs cannot occupy a hybrid orbital.arrow_forwardindicate 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.arrow_forwardConsider 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.arrow_forward
- The molecule shown below is called furan. It is represented intypical shorthand way for organic molecules, with hydrogenatoms not shown, and each of the 4 vertices representing acarbon atom. (a) What is the molecular formula for furan? (b) How manyvalence electrons are there in the molecule? (c) What isthe hybridization at each of the carbon atoms? (d) Howmany electrons are in the π system of the molecule? (e) TheC¬C¬C bond angles in furan are much smaller than thosein benzene. The likely reason is which of the following: (i) Thehybridization of the carbon atoms in furan is different fromthat in benzene, (ii) Furan does not have another resonancestructure equivalent to the one above, or (iii) The atoms in afive-membered ring are forced to adopt smaller angles than ina six-membered ring.arrow_forwardChloral (Cl₃C—CH=O) forms a monohydrate, chloralhydrate, the sleep-inducing depressant called “knockout drops”in old movies. (a) Write two possible structures for chloral hy-drate, one involving hydrogen bonding and one that is a Lewis adduct. (b) What spectroscopic method could be used to identify the real structure? Explain.arrow_forwardH genistein HO, H H : ОН HO, H (a) Is the hybridization of each C in the right-most ring the same? Explain. (b) Is the hybridization of the O atoms in/on the center ring the same as that of the O atoms in the OH groups? Explain. (c) How many carbon-oxygen o-bonds are there in genistein? How many carbon-oxygen n-bonds? (d) Do all the lone pairs on the oxygens occupy the same type of hybrid orbital? Explain by labeling the hybridization of each oxygen atom in genistein.arrow_forward
- (b) Draw the Lewis structure of the following molecule including its proper geometry. CH2CHC(O)CH3 a) Draw a complete orbital picture of the molecule.arrow_forwardButadiene, C4H6, is a planar molecule that has the followingcarbon–carbon bond lengths: (a) Predict the bond angles around each of the carbon atoms and sketch the molecule. (b) From left to right, what is the hybridization of each carbon atom in butadiene? (c) The middle C—C bond length in butadiene (1.48 Å) is a little shorter than the average C—C single bond length (1.54 Å). Does this imply that the middle C—C bond in butadiene is weaker or stronger than the average C—C single bond? (d) Based on your answer for part (c), discuss what additional aspects of bonding in butadiene might support the shorter middle C—C bond.arrow_forward3) Which statement best describe the structure of a carbonate anion C02- ? A) The electron geometry of carbon in a carbonate anion is trigonal planar with a sp2 hybridization and bond angles are 120°. There is a n-bond formed between a non-hybridized "C" p-orbital overlapping with an "O" p-orbital. C) The electron geometry of carbon in a carbonate anion is trigonal planar with a sp2 hybridization and bond angles are 120°. There is a 7-bond formed between a non-hybridized “C" p-orbital overlapping with an “O" p-orbital.arrow_forward
- Chemistry: Principles and PracticeChemistryISBN:9780534420123Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward MercerPublisher:Cengage Learning