1. Draw the HOMO and LUMO for the given molecule. Explain how bonds would change as you excite this molecule with UV/ Visible light. Be specific.
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- Draw Structure after.. 3) Flipping the molecule around 4) Rotating the molecule by 180 degrees AND flipping it around3. Draw an orbital overlap model of the following molecule and indicate the most reactive electron pair. Explain your reasoning based on VB theory.Use the following molecules to answer the worksheet.
- 1. Draw the HOMO and LUMO for the given molecule. Explain how bonds would change as you excite this molecule with UV/ Visible light. Be specific. bya model of each molecule shown above: Is the molecule in the left box the same moleculeas the molecule in the right box? Use your models to answer the question, and recall that...Could we cut just one bond in the "starting" molecule shown in the drawing area below to create this "target" molecule? The target molecule. If so, highlight the bond to be cut. If not, check the box under the drawing area that says Not possible. Note: it's OK if cutting the bond creates more than one molecule, as long as one of them is the target molecule. X
- Could we cut just one bond in the "starting" molecule shown in the drawing area below to create this "target" molecule? If so, highlight the bond to be cut. If not, check the box under the drawing area that says Not possible. Note: it's OK if cutting the bond creates more than one molecule, as long as one of them is the target molecule. Not possible. The target molecule. H H Note for advanced students: what we mean by "cutting" the bond here is breaking the bond and attaching H atoms to each dangling end, like this: ++*++ H C-H H-ő-H H X -Ö-H Se. Draw the cis and trans isomer of the molecule above. f. Draw the chair form of the cis isomer of the molecule. g. Draw the flipped chair form of the cis isomer of the molecule. h. What is the more stable chair form?A. Choose the letter of the best answer. 1. What is a saturated hydrocarbon? A. Any compound consisting of carbon and hydrogen only. B. Any compound consisting of carbon and hydrogen and oxygen only. C. Any compound consisting of carbon and hydrogen only, in which some of the carbon atoms are joined to each other by double or triple bonds. D. Any compound consisting of carbon and hydrogen only, in which all the carbon atoms are joined to each other by single bonds. 2. What kind of hydrocarbon is C3H14? A. alkane C. alkyne B. alkene D. alcohol H. H H. 3. This molecule is an example of an... H. A. alkane C. alkyne B. alkene D. alcohol 4. Which is an example of an ether? А. CН3ОН B. CH3CH2CH2CI C. CH3CH2OCH2CH3 D. CH3CH2COOCH3 5. What is the simplest organic compound? A. methane C. ethanol B. acetone D. ethane
- Please label all bond stretches in this molecule.match to the corresponding moleculeBenzene is the simplest member of a whole class of compounds called aromatic hydrocarbons. benzene a. How is each carbon atom hybridized? b. What is the geometry around each carbon atom? What is the overall geometry of the benzene ring? c. Draw a diagram showing the orbitals used to join the carbon atoms of the ring. d. Follow the indicated curved arrow notation to draw a second resonance structure. e. Benzene and other aromatic hydrocarbons are shown in Chapter 17 to be very stable. Offer an explanation.