Would this proposed synthesis work?
- What if I replaced pyridine with AlCl3?
We need at least 10 more requests to produce the answer.
0 / 10 have requested this problem solution
The more requests, the faster the answer.
Would this proposed synthesis work? - What if I replaced pyridine with AlCl3? 2 nor کم...
_____________> 1. CH3Cl, AlCl3 2. (i) KMnO4 (ii) H3O+ 3. CH3CH2CH2Cl, AlCl3 what are major products? Please explain step by step. Br
How do these synthesis problems work? What would the reaction be after each step? rf 1. S03 Ctt 3 i. SOる 2. IO 0
How would I do this synthesis ? What reagents would I use ? Using substitution and elimination. ilii OH
What reagents would I use? What would the synthesis look like? OH t enant oner
okay i attempted it, now just need help with this to check my work 2. Write the name of the following compounds: (Smith 9.3) Алісн сн. OCH_CH_CH3 P/12 PBr3 H.C, CH.CH TOH HCI TSCH pyridine он SOCI, pyridine SOCI
I was wondering what reagents would be needed to do the following synthesis? thanks! ? ? -NHCH3
ll Reep y eyes on my own work. I will not permit my work to be copied by others 3. I have neither stolen nor this quiz prior to the quiz time lg the quiz, and in particular if I leave for the washroom, I will not check course material on an electronic device or writen notes 6. I agree that actions described in points 2 through 5 are profoundly dishonest and dishonourable. They represent academic offences that can lead...
What reagents, out of those below, would allow the most efficient synthesis of CH3CH2CH2CH2C=CH from CH3(CH2)50H? Select all that apply. Part 1: A. HgSO4 B. POClz in pyridine Ос. Nан D. H202 E. H2S04 (2 equiv) F. HBI G. Cl2 H. KOC(CH3)3 (2 equiv) in DMSO 1. CH3CI J. BHz We were unable to transcribe this image
Can you answer them all? Thanks 10. What would be the product of the following reaction sequence? 1. CHJ (excess) 2. Ag O, H2O 3. heat но C. a. (HC)N e. mixture of (c) and (d) d. N CH3 CH3 CHg 11. Which of the following would fail to produce an ester? HO0 RCO H excess EtOH b. 1. DIBAL isopropanol CN C. d. CI 2. HO pyridine e. all of these will yield an ester 12. What would be...
Synthesis using Carbonyla-Substitution Chemistry Preamble This experiment involves the synthesis of target molecules using a-substitution chemistry. You are assigned two target molecules, one of which is best synthesized by an alkylation approach, while the other is best synthesized by an addition or condensation approach. My two target molecules are number 2 and number 12 in the last page. You must do the following: 1. Perform a retrosynthetic analysis on the two target molecules assigned to you. In each case the...