As OH- is a good source of electron i.e neucliophile hence it's gives electron to the electrophilic carbon center by knocking out l- which is a very good leaving group .
The reaction proceed via Sn2 mechanism as carbon is 1 degree.so I-can't leave the system before the attack of OH- .
please explain why/how the electrons flow in this reaction her HO: me + C I-O-I :...
Chemistry help, please explain how I get these please 4. Determine how many valence electrons come from each subshell in the following atoms: Atom Pin PO O in PO Total Valence s-electrons p-electrons d-electrons f-electrons Electrons 2 6 a 2 C 2 7 2 o Ir Cf .
Product(s) HO CH2 Predict the product(s) of this reaction by interpreting the flow of electrons as indicated by the curved arrows.
Please help me learn how to work out this problem. I assigned valence electrons but i keep having too many. Structure, Hybridization, Resonance, Aromaticity In which of these Lewis structures would the iodine be assigned a formal charge of +2? ST-2 (A) CH-i-ö CH厂1-0: (D) CH -に。 (C) CH,O--0
And explain why please. Problem 3.5 A stream of electrons (mass me and charge e) is accelerated (roughly from rest) through a potential difference created by a power supply of some EMF E. It then enters a region containing a magnetic field of strength B, as well as a pair of parallel plates of some separation h, which are charged by the same power supply. The strength of the power supply is then tuned until the electron stream continues through...
please explain How can this transformation be accomplished? OTS ?, A. Bry/CCI: B. H./Pd-C c. O/CHOH D. Br /HO H.B-H G. H.0 /acid I. H.O/NaOH F.H.O E. Zn K. NaH J. CI/H0 L. mCPBA M. H.SOJA N. TsCl/py 0. KMnO/KOH [A] H then M P. NaOH [B] D Q. HO/H.SO [C] O [D] P then B [E] K Explanation for your choice (3 pts)
Can someone please explain to me how they drew the nodes from the graph? Why and how did they know how to draw it? Also, someone show me different scenario for 2s or p and d and f? e2125) 4144 Hp HA He HA bding (151-150 Hs HA Ho HA nde L/ ant-loading 12s) (ISAT 10
Can someone please explain why the ordering is A>D>B>E>C I know why c is first because it's primary and why A is last because it's tertiary the most stable but the middle is hard for me to understand. Reaction coordinate 2. Rank the following carbocations in order of decreasing stability
please help me write mechanism of this reaction and explain why I observed the bromine dissolved in dichloromethane when added to the alkene the solution changed to light yellow. 3. Write a chemical equation for the test for unsaturation (Part B) using one of the possible alkenes above. What observation is made for a positive test and why? Explais Brz CH,CeZ The bromine dissolved in dichloromothane added to the alkene changed to light yellow, indicated a Postive resut
Please explain why only II will proceed. I am having difficulties understanding these questions, thank you! A16 Which of the following reactions would proceed as written? O - T 1. LiAIH4 2. HCI, H20 Me H MeoH Et 1. EtMgBr Me H 2. HCI, H Me OH 1. EtMgBr 2. HCI, H20 Et Me Me OH Me H MeH 1. NaBH4 2. HCI, H,Ó Me OH Tand II. A) B) C) D) E) Tand III. only. Ill only. IV only.
please explain, tell me, and show me how and why the answer is D? 9. What are the Cahn-Ingold-Prelog configurations at C(2) and C(5) in Penicillin G? SCHE a) C(2) is R and C(5) is R c) C(2) is S and C(5) is LYCH N -2 CH3 1 2H b) C(2) is R and C(5) is S d) C(2) is S and C(5) is R COH Penicillin G O