Draw resonance structures for the conjugate base that is produced when the following compound is treated with sodium ethoxide.منةOEtThere are THREE significant resonance structures for the conjugate base of this compound. Modify the given copies of the originalcompound to draw the resonance structures (no curved arrows are needed, and lone pairs do not have to be drawn). Use the +/- toolsto add/remove charges, and use the single bond tool to interconvert between double and single bonds.H3CH3CH3CEdit DrawingCH3CH3CH3

Answered: Image /qna-images/answer/ef4fb913-ff1c-4007-91da-7a4171420db3.jpg

Answered: Draw resonance structures for the…

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter20: Acidity And Pka Of Phenols

Section: Chapter Questions

Problem 20CTQ

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Similar questions

For the following molecules, identify the acidic hydrogens from among those that are bolded. For each acidic hydrogen that you identify, draw the conjugate base that results from a base removing that acidic hydrogen. For molecules with more than one acidic hydrogen, draw a separate conjugate base for each one.
For each of the following pairs, indicate the stronger and weaker acid by dragging the appropriate label under the structure.
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.
Rank the following compounds in order of increasing acidity (1 = least acidic, 3 = most acidic) and in the space provided use resonance (of the conjugate base) to explain why the compound you have labelled “3” is the most acidic.
Rank the following compounds in terms of increasing acidity (least acidic first). Explain your ranking. Making sure to say which hydrogen in each molecule is the most acidic, and discuss the relative stability of the conjugate bases.
The Ka of acetic acid (CH3CO2H) is 1.8x10-5 and the Kb of methylamine (CH3NH2) is 4.4x10-4. Complete the following equilibrium reaction (acid-base reaction) equation and predict the side of the equilibrium that is favored. Explain. Show all your work.
Please answer this NEATLY, COMPLETELY, and CORRECTLY for an UPVOTE. Arrange the intermediates below in order of increasing basicity:
Amides are weak nucleophiles but their conjugate bases are string nucleophiles. The amide drawn below can be deprotonated in four possible locations, labeled A-D but two are considerably more acidic than the others. Draw the two different Bronsted Lowery acid/base reactions (using HO- as the BL base) showing the deprotonation at these two locations. Draw all RS with arrows for both conjugate bases but no hybrids. Based on your resonance analysis which location is the most acidic in the molecule? Why is it most acidic? Amides can also be protonated by a strong acid in two different locations. Draw two different conjugate acids for the amide above as well as RS with arrows for each. Based on your resonance analysis which atom is the most basic in an amide?
Explain with the help of resonance structures which of the two nitrogen atoms is more basic in the following molecule.
Why is the chlorine in the ortho position less acidic than the one in the para position? Please explain in detail.
For each of the following compounds, draw the conjugate base. Use the conjugate base to explain in a sentence which of the original compounds will be the most acidic
Arrange the compounds in each set in order of increasing base strength. consult Table 4.1 for pKa values of the conjugate acid of each base.

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