
I re-did it and got same compound. Can someone show me how to get the answer to this one? assign R and S configurations.

I re-did it and got same compound. Can someone show me how to get the answer...
how would you name this compound. specifically the rotation
portion(R and S)
on my attempt i got mostly everything right except for the
configurations. (blue ink indicates a reversal of the rotation if H
isnt in the back.)
s for each of the following. CHs (b) Br e following organic halide R-93) tbeane Frethy layclokyare Br Br HCKC
Can someone explain this please? I got completely the opposite
answer
Stereolengo The following reactions were taken from thesywhesis of TTN. нсон, CH₃ : Ph O ОН о Pho OH 0 Compound H Me Me Me Me Compound G 2) BF3 Et,0 no Stereocenter Me Me Compound I = Compound J A asymmet!! Which compounds in this reaction are chiral? (Circle all that apply.) 2pt Compound G Compound H Compound Compound J How are Compounds I and J related to...
Hi.
Can someone explain to me what I did wrong ? Is it not the correct
newman projection ? How do I draw it right ?
I’m posting what my teacher did as well ! Thank you !
eliminationProdu Aeaction fhedict tollowing RD Stronj 6ase E 2 Me Stereospecitic MC CI Me MC et Me product is double bond IN frans fhic ense 3 -rotate c CH3 ナCH3 H 3 RO CH CHS CH C
eliminationProdu Aeaction fhedict tollowing RD...
Can someone explain to me how I got the wrong answer. Should I
not have rounded it?
Incorrect Question 6 0/2 pts Calculate the rms velocity (m/s) of CO2 at 76°C. Enter your answer as an integer. 141
Can someone please show me how to do this? I feel like I did
something wrong.
10. The half life of radioactive 32P is 14.3 days. How long does it take for 100 mg of this isotope to decay to 5 mg? 093 h@)-.k, n(100
can someone show me how to do the work and explain it to me
15. How would you synthesize the following compound starting with optically pure (R) or (5)-2 HCN H,C, X CH3 A) (1) (R)-2-butanol + TSCI B) (1) (S)-2-butanol + TsCI C) (1) (S)-2-butanol + H2SO4 (heat) D) (R)-2-butanol + NaCN/DMSO (2) NaCN/DMSO (2) NaCN/DMSO (2) HBr (3) NaCN/DMSO
Can someone walk me through the process on how to get the
INVERSE Laplace transform of
Thank you I will upvote.
s(+r)
Can someone show me the mechanism for this and explain to me
how they got it. I dont undertsand what is happening. Thanks!
4FS Facy DPBM Figure 2. Tetrafuran derived from pentaerythritol (4FS) and diphenyl bismaleimide (DPBM) serve as building blocks for a cross-linked polymer via Diels-Alder reaction.
hi, did I do the second data correctly? also can someone help
me with the third data how to do it
II, DATA and RESULTS: A INITIAL SOLUTIONS: In the space provided, fill in the information for each of the initial aqueous solutions. Solution # ution Formu Ammonium Carbonate NH4 CO Clear Barium Acetate(C CH COO Ba Calcium Chloride CaCl2 Ca Cl Clear Copper BromideCu(Br) Cu Br Bluish B) OBSERVATIONSDWrite general observations for each reaction, and state if precipitate (PPT)...
I got confused can you please explain to me how did he answer
this question, please I need to know in each step how did he do
it
Centre of Pressure Inclined Sluice Gate Example Bgate 2m 1.5m Hydrostatic force on sluice gate? Location of centre of pressure? Force on catch? 1.8m 45 Catch 1.5m 0- 45°. 2 13.02m x2x (1.8) S 12 3-02 (3x2) Fateh っ M.