4. Follow the prompts below to determine if the following molecules are aromatic, nonaromatic, or antiaromatic? a. Draw Molecular Orbitals for the triangular pi system. The nodes are given below to get you started. Add shaded orbitals and determine the number of constructive and destructive interactions for each. b. Place the three MOs on an energy diagram and determine the non- bonding line. c. One of the molecules below does NOT have a complete cyclic pi system? Which one? d. Of the other two molecules, one is aromatic. Which one and why? A
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- Click on all of the atoms that make up the largest coplanar unit in the molecule below. H. H. :C. H. H. H. H. C. H. H. H. Submit Answer Retry Entire Group 9 more group attempts remaining C-2. Provide the following answer using the following compound below. a. Assign the hybridization for each atom, except hydrogen. b. Determine the number of atomic orbitals and Molecular orbitals (AO, MO). c. Draw the atomic orbitals for each atom and their MO d. Draw the energy diagram. e. Assign the HOMO and LUMO in the energy diagram. H H-C-C=C-H :O: Ha.Determine the number of nodes and rank them in order of increasing energy. b.Draw the p atomic orbital contributions on each carbon atom (AO mixing pattern) that would give rise to the MO. c. Based on your answer to part (c) -determine whether each MO is overall bonding, nonbonding, or antibonding. Please explain steps
- 2. Provide the following answer using the following compound below. a. Assign the hybridization for each atom, except hydrogen. b. Determine the number of atomic orbitals and Molecular orbitals (AO, MO). c. Draw the atomic orbitals for each atom and their MO d. Draw the energy diagram. e. Assign the HOMO and LUMO in the energy diagram. H H-C-C=C-H FO: HMeet 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.The cations formed during 1,2 and 1,4 addition are different in energy due to their substitution patterns. True False
- 1. Do all of the following for each molecule or ion. a. Draw the Lewis Dot structure that minimizes formal charges. b. Draw the 3-D structure. c. Determine the Hybridization designation of the central atom. d. Determine the VSEPR designation. e. State what is its Molecular shape. f. Determine whether it is Polar (P) or Nonpolar (N). g. Determine the number of sigma (0) and pi (0) bonds in each structure А. РОд 3- B. SeF4 C. CH,O D. BrF5 Е. СН21. 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.For the structure below a. Identify the longest conjugated system you can.b. Draw a resonance structure using curved arrows in which you push electrons from one end of the conjugated system all the way to the other end.
- Show work with explanation needed of each options with structures...don't give Handwritten answer..don't use Ai for answering thisDraw an exact 3-D representation of the molecule from the model. please answer all question step by step. Answer follow image:3. Ror S determination. For each molecule below, determine if it is in the R or S configuration for the carbon atoms with the * using the rules discussed in class (and in the book), Write the configuration on the line BELOW the compound. HO H H. Br HN- CEN CF3 SH