A model for SO3 is shown in the chem3D window. SO3 has trigonal planar geometry. This issometimes called triangular planar geometry.ball & sticklabelsRotate the molecule until you have a feeling for its three-dimensional shape. How many atoms arebonded to the central atom?|Consider the bond angles at the central atom. Do they all have approximately the same numericalvalue?What is the approximate numerical value of this angle?(| degrees.For practice, type in the name of the geometry of the molecule:

Answered: Image /qna-images/answer/4b86dc00-0539-4afc-9552-5e6a01580a81.jpg

Answered: ball & stick labels Rotate the 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

Chapter10: Molecular Structure And Bonding Theories

Section: Chapter Questions

Problem 10.118QE

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Similar questions

Consider the following flat drawing of methane (CH4) . a. What is HCH bond angle implied by this drawing if you assume it is flat? b. Are the electron domains of this flat CH4 spread out as much as possible? c. Use model materials to make a model of CH4 (methane). If you assembled it correctly, thefour bonds (bonding electron domains) of your model will be 109.5° apart. d. In which representation, the drawing above or the model in your hand (circle one) are theH’s of CH4 more spread out around the central carbon? e. Confirm that your model looks like the following drawing. The wedgebond represents a bond coming out of the page, and the dash bondrepresents a bond going into the page f. You will often see methane drawn as if it were flat (like on the previous page). Why is thismisleading, and what is left to the viewer’s imagination when looking at such a drawing?
For each of the following molecules, complete the Lewis structure and use the VSEPR model to determine the bond angles around each central atom. Note that the drawings are only skeleton structures and may depict the angles incorrectly.
A student draws the picture of ammonia (NH3) in the box below, left, and predicts it will be a flatmolecule with HNH bond angles of exactly 120°. Unfortunately, the student left something out. a. What did the student omit from his drawing? b. What is the actual HNH bond angle of ammonia (based on the draw g above, right)? c. Explain why water, ammonia, and methane (shown below) all have about the same bondangles (close to 109.5°) even though they have different numbers of bonds.
In each of the following molecules, a central atom is surrounded by a total of three atoms or unshared electron pairs: SnCl2, BCl3, SO2. In which of these molecules would you expect the bond angle to be less than 120? Explain your reasoning.
Compare Figs. 4-47 and 4-49. Why are they different? Because B2 is known to be paramagnetic, the 2p and 2p molecular orbitals must be switched from the first prediction. What is the rationale for this? Why might one expect the 2p to be lower in energy than the 2p? Why cant we use diatomic oxygen to help us decide whether the 2p, or 2p, is lower in energy?
Why do we hybtidize atomic orbitals to explain the bonding in covalent compounds? What type of bonds form from hybrid orbitals: sigma or pi? Explain.
In Chapter 6, we study a group of organic cations called carbocations. Following is the structure of one such carbocation, the tert-butyl cation. (a) How many electrons are in the valence shell of the carbon bearing the positive charge? (b) Using VSEPR, predict the bond angles about this carbon. (c) Given the bond angle you predicted in (b), what hybridization do you predict for this carbon?
trans-tetrazene (N4H4) consists of a chain of four nitrogen atoms with each of the two end atoms bonded to two hydrogen atoms. Use the concepts of steric number and hybridization to predict the overall geometry of the molecule. Give the expected structure of cis-tetrazene.
Numerous molecules are detected in deep space. Three of them are illustrated here. (a) Are these compounds isomers? (b) Indicate the hybridization of each C atom in each molecule. (c) What is the value of the HCH angle in each of the three molecules? (d) Which of these molecules is/are polar? (e) Which molecule should have the strongest carbon-carbon bond? The strongest carbon-oxygen bond?
Use Figs. 4-54 and 4-55 to answer the following questions. a. Would the bonding molecular orbital in HF place greater electron density near the H or the F atom? Why? b. Would the bonding molecular orbital have greater fluorine 2p character, greater hydrogen 1s character, or an equal contribution from both? Why? c. Answer the previous two questions for the antibonding molecular orbital in HF.
If you have three electron regions around a central atom, how can you have a triangular planar molecule? An angular molecule? What bond angles are predicted in each case?

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