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- Orgonic Chemistry II: The answer is writtten as followed. But I Need Explanation. My question is that: Can I siwtch reagent 2 to reagent 1? for example reagent 1 is Cl2,Fecl3, can I changed it to reagent 2??? Why and why not???3. Based on the definitions of the terms below select the best classification for the following reactive species below: nucleophile; electrophile; free radical; carbocation; carboanion, electron rich species, delocalized electrons (i) CH3-: …………………………………………(ii) Br ∙ : …………………………………………. (iii) H2O : …………………………………………. (iv) CN- : ………………………………………….(v) Cl+: …………………………………………….(vi) CH3CH2+: ……………………………………..(vii) CH3∙ : …………………………………………… (viii) CH2CH2 : …………………………………………..a) b) c) d) e) 1) BH3/THF 2) H₂O2 NaOH (aq) cold Cl₂, H₂O HBr CH3CH₂OOCH₂CH3 1. Hg(OAc)2, H₂O 2. NaBH4 o 1) 03 (-78 °C) 2) (CH3)S H₂ Lindlar catalyst
- d) e) H₂CN NH ره b ...ОН OH H CH₂ 1. (CH3)₂CHMgBr, ether 2. NH,C1, H,O .CH, CH₂OH Products Products "c H Br. ü OH H ¹0 CH₂ شده NH Br. oły OH OH CH₂ CH,I have this task in organic chemistry (book: Brown's introduction to organic chemisty, global edition). Task 10:42. In (a) I have to tell what the funcion of K2CO3 is in step 1. Is it that CO32- take the hydrogen atom in 1-napthol? Will it then be a SN2 mechanism? In (b) I have to name the amine used in step 2 to form Propanolol. But I can't really find out how to come up with an amine that will make that reaction. Here are two pictures of the task:2. Label the following reactions as most likely occuring by an SN1 or SN2 mechanism. Explain your answer. (4 marks) HBr A) HO, CH;CH2OH 'Br B) Na* SCH; CH;CN ‚Br „SCH3
- Electron pairs CH3 .. Erase H3C - С — СІ: H3C – S- CH3 CH3 CH, CH3 THF/H,0 + H,C--CH, CH C- CH CHs CH, Use curved arrows to write the first step of this nucleophilic substitution mechanism. :ö: | :ö:f) 5) 2. Synthesis b) c) a d) > .On CH3 CHO СН3-С=Сн .OH COM инг 1) CrO₂, H₂ sop 2) , 3) H₂, Pd-c 1) LiACH & (excers) 2) Tsll, Pyridine (209) 3) конви (чод) 7 cipt Асоон nisł CH3-CE IZ H 2 ofWhat is the Potential energy diagram for this reaction. Pls draw with as much detail as possible. labels and scale) 2-methylpropan-2-ol ---> 2-methylpropene +H2O Draw the potential energy diagram for the reaction of 2-methylpropan-2-ol ---> 2-methylpropene + H20 (1) Label the structures of the (a) reactants, (b) intermediates, (c) transition states, (d) products, and (e) activation energies (E.) for each step. (2) Which step is the rate-determining step? (3) Identify the electrophile and nucleophile in each step when applicable.
- draw 5-hexyl-2-methyl-4-(2-methylprop-2-enyl)octa-1,7-diene ..............................Use the E2 mechanism to explain why when I is mixed with sodium ethoxide (NaOEt) in ethanol, the major product is III, but when II is mixed with sodium ethoxide in ethanol, the major product is IV. H3C CH3 H3C CH3 ..CI CI CH3 I CH3 || H3C. CH3 H3C CH3 E ||| CH3 CH3 IV SANHow many and what type of products will form if the following molecule undergoes E1? H Br choose your answer... V total product(s) form. choose your answer... V will be optically active.