Question 1: Aromaticity a. Draw a fully labelled MO energy diagram for each (match clearly). b. Determine criteria for the following molecules that aligns with the criteria for aromaticity. I will NOT accept anything outside the list done in class – NOTHING YOU HEARD FROM SOMEONE OTHER THAN ME, READ OR SAW ONLINE. List clearly for each molecule the way we did in class. c. Determine if the molecule are aromatic or antiaromatic based on your list. d. Of the two molecules, which would be most reactive in an electrophilic addition? Why?
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- 2. Find aromatic, antiaromatic and non-aromatic species among the following. Draw an energy diagram of the following species, where the species should be on the x-axis and energy will be on the y-axis.Draw an exact 3-D representation of the molecule from the model. please answer all question step by step. Answer follow image:Circle any of the following which you think are aromatic systems. For the ones that are aromatic systems, give the "n" (Huckel number.) It's possible tk have more than one. Thank you!
- Which arrow (x, y, or z) points toward the most acidic proton in the molecule to the right? (Arrows pointing toward C can be assumed to point at the H attached to that C.) Which structural feature plays the most significant role in influencing the relative acidities of the indicated protons? a. inductive effect b. size c. resonance d. hybridizationMeet benzylpenicillin, a common antibiotic for bacterial infections. Answer the following parts about this compound. a. Label all the functional groups present. b.For every heteroatom (i.e.atoms that are not CorH),predict the expected hybridization. c.Circle every carbon with a hydrogen capable of participating in hyperconjugation with a double bond. d.Draw one key resonance structure for each functional group capable of resonance, and one resonance hybrid with partial charges as applicable. e. Give the IUPAC name for this compound. Just kidding! It’s 3,3-dimethyl-7- oxo-6-(phenylacetamido)-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid. Now, sit back and appreciate the limitations of naming—it’s only useful insofar as we understand each other.1. Add nonbonding electron pairs to each atom where it is implied by the line-angle drawings shown below. 2. Use the curved arrow formalism to generate four additional, valid resonance structures for each compound. 3. Rank your resonance structures in order of increasing contribution to the overall nature of the molecule.
- | Determine whether the following molecules are aromatic (A), non-aromatic а) (NA), or anti-aromatic (AA). Please provide your answer on the line below each molecule. Additionally, include the total number of conjugated p-orbitals in each molecule (not pi- electrons!) conj. p-orbitals - conj. p-orbitals - conj. p-orbitals conj. p-orbitalsHi. I have trouble to answer this question. Help to label each compound B-E as an isomer or resonance structure of compound A.. could you explain to me in details how it be especially for each isomer , please indicate what bonds differ from compound A.. Thak you for your help.1. Is the molecule below aromatic? If so, circle the atoms that are part of the aromaticity. Also indicate the orbital that each lone pair occupies. .N. H2N
- 4. Which of the following species are aromatic or anti-aromatic (assuming n-systems are fully planar)? Circle those that are aromatic Put an X through those that are anti-aromatic Do nothing to the structure otherwise 5. Which of the following compounds will have the larger Amax ? Briefly explain in terms of MO theory and photon energy & basic wave property equations. 6. For the allyl anion below, A) Draw the second resonance structure and show the arrow-pushing needed to get to that structure. B) Draw the Valence Bond Theory Orbital Overlap Diagram of the resonance hybrid C) Make an Aufbau diagram of the relative energies of the n molecular orbitals, distribute the electrons of the p orbitals to the MO's, and label the MO's as r, mb, and ri (molecular orbital theory) D) Sketch the shapes of the 3 molecular orbitals in part C.4. Determine if the molecules below are aromatic, antiaromatic, or nonaromatic. If it is not aromatic, explain why.Be sure to answer all parts. Hydrocarbon A possesses a significant dipole, even though it is composed of only C-C and C-H bonds. Part 1 out of 2 Complete a resonance structure of the above molecule so that the positive pole is on the left and the negative pole is on the right. Hint edit structure ... Solutic 2 attempts left Check my work Next part Guided So