Draw significant resonance structures for the following compound: Step 1 First, add curved arrow(s) to show the resonance using the following pattern: an allylic carbocation. Mod given to draw the new resonance structure. Include lone pairs and charges in your structure. Use the + ar to an atom, and use the single bond tool to add/remove double bonds. CH3 CH3 Edit Drawing а CH3 CH3
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- Sketch the MO diagram for 1,3 budadiene. Determine the net bonding interactions for ¥2 and ¥3. How many nodes are in ¥4? How many AO’s were used? How many MO’s resulted?please determine the bond orders and compare the bond lengths of N2, N2-, and N2^2-species Using molecular orbital (MO) energy-level diagram,pKa = 9.6 pK, = 2.3 H :0: || H-N- C-C-Ö-H H 120° 180° H H 20. 105° The structural formula of the glycinium cation is shown above. Arrows indicate the pka values for the labile 90° protons in the molecule. CLEAR ALL What is the approximate H-O-C bond angle in the glycinium cation? +
- Draw the structure of the product that forms when the carbonyl compound shown is treated with K₂ Cг2 О7. If no reaction occurs, draw the structure of the organic starting material (reactant). CH3(CH2), (CO)CH (CH3)2 Click and drag to start drawing a structure. : ☐4-methyl-2-penteneUse Frost Circles to complete the molecular orbital diagram for cyclooctatetrane. Label the bonding, non bonding, and anti bonding MO’s. If the molecule is planar, would it be aromatic, antiaromatic, or nonaromatic? If the molecule is nonplanar, would it be aromatic, antiaromatic, or nonaromatic?
- Calculate the charge and draw the structure of the predominant ion for: (i) Lysine at pH 7.0 (R=-CH2CH;CH;CH¿NH2) (ii) Glutamic acid at pH 7.0 (R=-CH2CH;COOH) (iii) Serine at pH 1.0 (R=-CH2OH)Convert the following structural formulas into condensed structures.H₂C-C Ö: CH2 H3C — с O CH₂ + Clear The Lewis structure of acetone enolate ion, which has one other resonance structure, is shown. Complete the resonance structure by dragging bonds, charges, and electron lone pairs to their appropriate positions. Then check your answer.
- In the following questions, consider the carbanion formed by the arrow pushing below: он | HC-C-R H ཋཙམཏིཏཡརིཡཐཱ པཱལཾ ཏིཡཏིཡ, B: H C-C-R Н Question 7 2 pts Below are a proposed resonance structure of the carbanion and rules of resonance. Which rules, if any, does the resonance structure break? (Select all that apply.) Ο Η | │ C-C-R H The formal charge of the molecule cannot change. ☐ Single (sigma) bonds cannot be broken. With the exception of carbocations, octet rules must be satisfied. ☐ All of the above rules are satisfied.Be as detailed as you can possibly be.VISUALIZE The structures depicted are (a) enantiomers (b) different views of the same molecule (c) geometric (cistrans) isomers (d) both geometric isomers and enantiomers (e) structural isomers