Please click on the image if the problem isn’t showing up on default. Thank you :) Draw all significant resonance structures for the following compound:Step 1X Your answer is incorrect.First, add curved arrow(s) to show the resonance using the following pattern: an allylic lone pair. Modify the second structuregiven to draw the new resonance structure. Include lone pairs and charges in your structure. Use the + and - tools to increase ordecrease the charge on an atom, and use the single bond tool to add/remove double bonds.

By movement of free electrons through the pi bonds form resonating structures.

Answered: Draw all significant resonance…

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter4: Polar Bonds, Polar Reactions

Section: Chapter Questions

Problem 11CTQ

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Similar questions

Draw all significant resonance structures for the compounds shown below and use curved arrows to show the movement of electrons. You may need to add lone pairs. Circle the most significant contributor in each case. Explain why it is the most stable.
Name the following unbranched molecules from the numbered cards. When using a locator number use a dash to separate the number from the name. Type all answers in lowercase letters only. Name cards: 3,4,7,8,12,13,16,18,19,20,21,26
Instructions: Make sure to make your explanations precise and show your complete solutions. Thank you Draw a labeled molecular diagram to explain how the Law of Mass Conservation applies to the chemical reaction below. ?? + ??? → ? ??? Make sure to label each atom/molecule on the reactant and product side. You may draw arrows to indicate bond formation or zigzag lines to indicate breaking of bonds.
(1, 7) Draw both resonance structures of the anion formed by the reaction of the most acidic C-H bond of the compound below with base. Include all valence lone pairs in your answer. For structures having different hydrogens of comparable acidity, assume that the reaction occurs at the less-substituted carbon. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate resonance structures using the ↔ symbol from the drop-down menu.
Please draw a more stable resonance structure for the following molecule. Use a curved arrow to show how to transform the original structure to the new one and please specify charges.
Draw two resonance structures better than this. Include curvy arrows to show how you determined the structures. Lone pairs are not shown so include lone pairs in the original and subsequent structures. Label the major, minor, and very minor contributors.
Draw a more stable resonance structure for the following molecule. Use a curved arrow to show how to transform the original structure to the new one and please specify charges.
A. Draw the major resonance structure, then draw curved arrows to show how this can be converted to the Lewis structure given. B. Thionitromethane is redrawn for you. Draw curved arrows to show how this can be converted to the resonance structure you drew in part A.
Draw all resonance contributors for each of the following molecules or ions. Be sure to include the curved arrows thatindicate which pairs of electrons are shifted in going from one resonance structure to the next.(a) CH3NO2(b) CH3CO-2(c) CH3CHCHCH-2(the ion has two C-C single bonds)(d) C5H5N (a ring is formed by the C and N atoms, and each H is bonded to C)(e) C4H5N (a ring is formed by the C and N atoms, the N is bonded to one H, and each C is bonded to one H)
Draw the structures of the products of the neutralization reaction between methylamine and propanoic acid. Include all valence lone pairs in your answer. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate multiple products using the + sign from the drop-down menu.
Add the curved arrow(s) to each resonance structure that are necessary to convert it to the next structure. (The final resonance structure requires no curved arrows.)
An electrostatic potential map of calicene is shown below. a) Both the electrostatic potential map and its significant dipole moment indicate that calicene is an unusually polar hydrocarbon. Which of the dipolar resonance forms, structure A or structure B, better corresponds to the electron distribution in the molecule? Select the single best answer. b) Which one of the following structures should be stabilized by resonance to a greater extent? Select the single best answer.

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