lease explain the answer Chlorine is an CIRCLE one ortho-para or meta director. Please include, show all resonance contributors after chlorobenzene loses aromaticity to form a sigma complex. To save time: If your answer is “ortho-para” director, just show addition at either position. If your answer is “meta” director, just show the result of meta addition.

lease explain the answer Chlorine is an CIRCLE one ortho-para or meta director. Please include, show all resonance contributors after chlorobenzene loses aromaticity to form a sigma complex. To save time: If your answer is “ortho-para” director, just show addition at either position. If your answer is “meta” director, just show the result of meta addition.

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter13: Substitution

Section: Chapter Questions

Problem 26E

See similar textbooks

Similar questions

Chlorine is a(n) (CIRCLE one) ortho-para/meta director. Explain your answer. In your explanation, you must show all resonance contributors after chlorobenzene loses aromaticity to form a sigma complex. To save time: • If your answer is "ortho-para" director, just show addition at either position. • If your answer is "meta" director, just show the result of meta addition.
Explain your answer. Match the words in the left column to the appropriate blanks in the sentences on the right. Make certain each sentence is complet Submit carbanion E1 carbocation minor major E2 fluoride Request Answer Reset Help product would be the one The predicted by Zaitsev's rule, because the ion would dissociate in the first . Loss of a proton would follow Zaitsev's step, forming a from the rule, as it does in other reactions.
Examine the molecules below. Which site is most basic? Which H is most acidic? Highlight this site. Highlight this H. H :S- H. :O:
Draw the products of the reaction shown. Electron flow is indicated with curved arrows. • Include all valence lone pairs in your answer. . Include counter-lons, e.g., Na*, F, in your submission, but draw them in their own separate sketcher. • 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. +98) 24 Y SIF Next
Hi, I’m trying to complete the reactions by figuring out what RXNs these are. Can someone check my work please and tell me if I’m doing this right and provide and example like how I have drawn? Thank you!
Which arrow (x, y, or z) points toward the most basic atom in the molecule to the right? 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. hybridization
The structure shown below is has a very high pKa because the conjugate base is very unstable. Using the provided resonance structures, draw the curved electron-pushing arrows to show the deprotonation step. Then, draw the curved electron-pushing arrows to show the interconversion between resonance hybrid contributors. Be sure to account for all bond-breaking and bond-making steps. H Select to Add Arrows CH3CH2CH2CH2Li H Select to Edit Arrows H H LIⒸ
Answer the following problem.
[References) Identify the most and the least acidic compound in each of the following sets. Leave the remaining answer in each set blank. a) p-cyanobenzoic acid: v benzoic acid: p-aminobenzoic acid: b) 3-fluoropropanoic acid: fluoroacetic acid: | iodoacetic acid: c) acetic acid: fluoroacetic acid: chloroacetic acid: most least
Draw the products of the reaction shown. Electron flow is indicated with curved arrows. Ö: in . Include all valence lone pairs in your answer. • Include counter-ions, e.g., Na*, I, in your submission, but draw them in their own separate sketcher. • 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. 0- NH3 Ⓒ www. SIF
Be sure to answer all parts. Be sure to include the ion charges. Draw the products of each acid-base reaction. 1866qs draw structure ... + draw structure ... higher molecular weight product lower molecular weight product
Draw the mechanism showing the Brønsted acid/base reaction between propanoic acid and methylamine. Label the acid, base, conjugate base, and conjugate acid. Show all curved arrows, lone pairs and nonzero formal charges. HO. CH;NH2 methylamine propanoic acid pKa = 4.9 Mechanism: uerm lo noits adi ol maie Using the pKa information provided/pKa tables (table appended to the end of this document), determine whether the starting reagents (propanoic acid and methyl amine) or products would be favored at equilibrium (no math needed!).