need help with organic chemistry please show mechanism

Write the letter (case sensitive response) corresponding to the word/statement /structure that best fits to complete the statement below. Coupling of an alkene with ArBr or Arl under the influence of a Pd(0) catalyst is an example of A) Stille B)1,4 addition C) Allylic Radical addition D)Suzuki E) 4+2 cycloaddition F) Vinylic Radical addition G) Heck H) NAS J) Sigma complex K) EAS L) SN1 M) MO diagram reaction N) 1,2 addition P) SN2 Q) Frost circle

What does In-situ mean in the case of In-situ reaction? example down below Benzyne is a highly reactive organic molecule that has not been isolated. It is prepared in situ reaction. Its instability is the result of its triple bond.

Question 11 of 20 Submit Identify which of following alkyl halides undergoes solvolysis most rapidly. Br Br II Br A) I B) I| C) II Tap here or pull up for additional resources

I am having trouble witht this equations do you know how to go about it, i would appeciate the help

refer to image, answer in detail. will rate.

For these next two mechanism questions, do each step above the arrows one at a time. i.e. don't try and do them all at once OH 1. NaH (1 eq.) 2. 0⁰ 3. NaOH H₂O

TA-Conta.... Disney Movie Club Ho... phol Reactions i Be sure to answer all parts. Draw a stepwise mechanism for the following reaction: Part 1 out of 3 edit structure ... 2 attempts left Disney Movie Club Ho... GEnjoylfun Maps Gmail Translate Official Support | ASU... https://icr-am.asus.co... OH SOCI₂ pyridine edit structure. Check my work + O O CD HCI HOCI SO₂ HO CI +50₂ + HCI Saved Next part 252Fnewconnect.mheducation.com%252F /activity/question-group/KEZA New Tab Support for Dell Active... Feedback This is not a bad approach but the electrophile contains a good leaving group so rethink your answer and consider doing a substitution rather than an addition reaction. Hint Solution Guided Solution 12 Ok, got it

(Time constraint) Please provide the common name

Two curved arrows are required to complete the given mechanism step. Refer to the numbered atoms (1, 2 and 4) and the numbered bond (3), as needed, to describe the positions where each arrow starts (tail) and ends (head). Select all that apply. 0 0 0 0 0 0 0 0 N:O: 3 One curved arrow starts at 4 and ends at 2. One One One curved arrow starts at 2 and ends at 4. curved arrow starts at 4 and ends at 1. curved arrow starts at 2 and ends at 1. One curved arrow starts at 3 and ends at 2. One curved arrow starts at 1 and ends at 2. One curved arrow starts at 1 and ends at 4. One curved arrow starts at 3 and ends at 4.