(c) Use what you learned in Question 2 to illustrate each type of force that can exist between two methanol molecules. Hint: you have done this quite a bit already in lab and lecture. London Dispersion Dipole-Induced Dipole Dipole-Dipole Hydrogen-Bonding
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- Answer the questions below for 2,4-hexadiene. Before you begin, construct a molecular orbital (MO) diagram for the conjugated system. Number the MOs consecutively in order of increasing energy starting with 1 for the MO at lowest energy. a How many p atomic orbitals are in the conjugated system?Consider the product below a) Would this product show a signal in a UV-Vis spectrum? Why? b) Would this molecule have a non-zero alpha-value in polarimetry? Why? c) What stretches would be expected in an IR spectrum of this molecule? d) Predict the 1H NMR spectrum for this molecule. For H1 to H6 e) Predict the 13C NMR spectrum and DEPT spectra for Carbon A- Carbon G. Use (+) for positive signals, (-) for negative signals, and (X) for no signal in the DEPT NMR spectra. f) If a base such as NaOH was used, it would be harder to determine the major product before running the reaction. Once the reaction was run, how would you determine the product favored using spectroscopy?When drawing the resonance structures for a toluene carbocation (like the one attached below), should I include the structure created after a bond shift from the fourth structure, even though it mimicks the first structure? What about in the second picture- should the crossed out structure be included despite its similarity to the first one? Overall, I'm having trouble determining whether two compounds are the same and don't need to be drawn twice or just similar and need to drawn twice.
- Answer the last bullet point subpart question only.В. For each of the cases below, give an example. NO STICKS ARE ALLOWED. Please make sure I can "read" your structures. 8. An aromatic cyclic anhydride 9. Aromatic tertiary amine salt 10. Aromatic tertiary alcohol that also has a ketone group 11. Non-aromatic primary alcohol that also has an amide group 12. A hydrocarbon that is both aromatic and aliphatic 13. An aromatic that contains a trans group, as well as a meta-directing group 14. An aromatic that will NOT react with an acid halide 15. A para-substituted guy who can form a diazonium saltAmmonia is more polar than phosphorus trihydride. Provide an explanation. Of course, since this question is in the VSEPR lab and polarity is mentioned, it would help to draw the three dimensional geometry of each.
- practice q 13 13. Complete each of these following reactions (i.e. fill in the boxes with the missing reagent(s) or major product(s). Indicate the stereochemistry if applicable.The compound below is treated with N-bromosuccinimide (NBS) in the presence of light. Draw both resonance structures for the radical produced by reaction of the compound with a bromine atom. Assume reaction occurs o the weakest C-H bond. • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. Separate resonance structures using the symbol from the drop-down menu. Include all valence radical electrons in your answer. 000 PreviousGiven all the following information, please fill out everything i didn't I am trying to use this to study and I am very confused, everything I have filled out is correct I confirmed with my professor, but I am so confused on the rest of it