I got the first part of the question correct, but it is marking my resonance-stabilized intermediate as incorrect. Plea...
Draw the carbocation intermediate that is expected when each of the following alkyl halides undergoes ionization. In each case, if the carbocation is resonance-stabilized, make sure to draw the resonance structures. Include formal charges in your answer. Do not add curved arrow(s) or resonance arrow(s) in your answer if any. x Your answer is incorrect. Try again. Edit By accessing this Question Assistance, you will learn while you earn points based on the Point Pot
+ H2O Edit SHOW HINT SHOW ANSWER LINK TO TEXT Attempts: 1 of 3 used Part 2 Get help answering Molecular Drawing questions. The intermediate formed in the previous step is resonance stabilized. Draw the missing curved arrow(s) to convert the first resonance structure into the second one. Add any missing lone pairs of electrons. Attempts: 0 of 3 used SAVE FOR LATER SUBMIT ANSWER
Show all four resonance structures for the molecule shown. PRINTER VERSION BACK NEXT Question 12 HO-C-NH2 Practice Problem 02.62a Get help answering Molecular Drawing questions. Your answer is incorrect. Try again. The following cornpound has four significant lone pairs in your answer (including the initial structure shown). Modify the given drawings as needed to show all four resonance structures. Include formal charges and Edit HOCNH, o CNH, 0 CNH By accessing this Question Assistance, you will learn while you earn...
View History Bookmarks Window Help Chapter 2 Klein, Organic Chemistry, 3e Testbank, Question 128 Your answer is incorrect. Try again. Draw the curved arrow(s) for converting the first resonance structure into the second resonance structure. 0 0 Edit By accessing this Question Assistance, you will learn while you earn points based on the Point Potential Policy set by your instr 42 Question Attempts: 3 of 15 152 157 20 F5 F6 F7 FB
draw the mechanism as well please! with lone pairs Question 8 When the following ketone is treated with aqueous sodium hydroxide, the aldol product is obtained in poor yields. In these cases, special distillation techniques are used to increase the yield of aldol product. Predict the aldol addition product that is obtained, and propose a mechanism for its formation. For the mechanism, draw the curved arrows as needed. Include lone pairs and charges in your answer. Do not draw out...