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- 4. Explain why the following molecule is considered aromatic. (it may help to draw a resonance form) O:Draw a structure of oxindole, with an aromatic ring. Make sure the diagram contains sp3 carbon atom, sp2 carbon atoms, and sp hybridised carbon atoms. The structure should also include a sp2 hybridised heteroatom and a hybridised sp3.The aromatic energy diagram below corresponds to an anti-aromatic compound.?
- A single bond between two carbons with different hybridizations has a small dipole. What is the direction of the dipole in the indicated bonds?C. D. O: :O: The lone pair in compound C is Compound C is In compound D, not aromatic. aromatic. delocalized. not delocalized. one lone pair is delocalized. both lone pairs are not delocalized. both lone pairs are delocalized. CompoundCan you please explain why these are the ortho and para placements to the alkoxyl group?
- What type of atomic or hybridized orbital is each lone pair indicated below in? Compound A Compound B Compund A (unhybridized p-orbital) and Compound B (sp3-hybridized orbital) O Compund A (sp2-hybridized orbital) and Compound B (sp3-hybridized orbital) Compund A (sp3-hybridized orbital) and Compound B (unhybridized p-orbital) O Compund A (unhybridized p-orbital) and Compound B (sp2-hybridized orbital)o. Opioids are compounds derived from opium, which comes from the opium poppy. Although in reality, all poppies produce opoids, the drug “morphine" , codeine as well as other opioid pain killers are typically derived from opium. A quick way to find or identify these compounds is to look for a six-membered ring containing a nitrogen. Often, if you see a six-membered ring with a nitrogen, you have some sort of an opoid or a modified synthetic pain killer. With that said, morphine and codeine are typically not injected or given orally in pure form. Instead, their salts are used, such as morphine sulfate or codeine phosphate. Why are the salts used or administered instead of the pure substances (or non-salt forms)? (I am not interested in drug names, but to have you answer the why of this question.) BIU E E E E 3回fe 27 В. acen W 1 F T F2 F3 F4 F5 F6 F7 F8 F9 F10 F11 F12 () NumLk Prt Sc Pause BrQuestion 2. Draw the molecular orbital diagrams for thioazepine. Indicate if this compound is aromatic, non-aromatic or anti-aromatic using this energy diagram. Justify your answer. N S
- Draw a resonance structure, complete with all formal charges and lone (unshared) electron pairs, that shows the resonance interaction of the cyano with the ortho position in benzonitrile. CEN benzonitrile • You do not have to consider stereochemistry. • Include all valence lone pairs in your answer. • In cases where there is more than one answer, just draw one.or the molecule below, whic The molecule is aromatic The molecule is not aromatic The molecule is not aromatic O The molecule is not aromatic O We cannot determine if the meis this molecule aromatic answer by drawing orbitals (VBT), applying huckels law, and drawing frosts circle
