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- Thionyl choride, SOCl2, is a reagent commonly used to convert the –OH group of an alcohol to a better leaving group. What is the formal charge on S in this molecule? A) +2 B) +1 C) 0 D) -1 E) -2verse osis Consider the structures of the carbocations formed by ortho attack of the electrophile, *NO₂, on the given starting material. NH2 Part: 0/2 Part 1 of 2 + Draw all resonance structures for the carbocation formed by ortho attack of the electrophile "NO, on the given starting material. If applicable, include the resonance structure in which π bond electrons "move" to the more electronegative atom as a lone pair. Be sure to include all charges and relevant lone pairs. 00 al. Ar B KFirst Writedown which reaction it is? SN1, SN2, E1? Write a stepwise mechanism for the following reactions showing ALL intermediates. Use curved arrows to symbolize the flow of electrons to show how each of the intermediates and product are formed. Show all necessary lone pairs and formal charges.
- Curved arrows are used to illustrate the flow of electrons. Using the provided starting and product structures, draw the curved electron-pushing arrows for the following reaction or mechanistic steps. Be sure to account for all bond-breaking and bond-making steps. :OH: Select to Add Arrows H₂O 3 H₂ H HH H :Br:Ⓒ HH Select to Add Arrows H₂O 17 :Br: H H Please select a drawing or reagent from the question areaWhich of the following structures, including formal charges, is correct for diazomethane? H₂CNN: H₂C=N=N: H₂C N3 EN: H₂C=N= EN: +3 -3 7:2: H₂C-N- N:Which is a product of this reaction according to the arrows? All lone pairs and formal charges are shown. Additional products may be missing. O O O O A B U D A OCH3 OCH3 :: B ? OCH 3 :0 OCH3
- Q4 * 1,3-thiazolo[4,5,b]pyrdine 1,5-thiazolo[4,5,b]pyrdine 1,3-thiazol[4,5,c]pyridzine 6-thiabicyclo[4.5]decane 1-thia[5.6]decane Both are wrong Q5* ΟΟΟ Q6 * 2H-1,3-oxazete 4H-1,3-oxazete 2H-1,3-oxazane 4H-1,3-oxazaneUse the curved-arrow formalism to show how the electrons flow in the resonance form on the left to give the one on the right. Make the ends of your arrows specify the origin and destination of reorganizing electrons. Arrow-pushing Instructions Submit Answer m H Try Another Version 2 item attempts remaining a Use curved arrows to show how the alkene below will react with HCI. Make the ends of your arrows specify the origin and destination of reorganizing electrons. Arrow-pushing Instructions NA ↔XT H H3. For the following structures: CH3a C-CH,CH3 C Hy' H (a) Determine whether each radical is a primary, secondary, or tertiary radical. (b) Rank these radicals in terms of their relative stability (1 = most stable to 3 = least stable). 4 Draw the (2) banoggata 1o
- a) Please indicate whether the following molecules are aromatic, non-aromatic, or anti-aromatic. In those cases where a resonance structure is required to achieve aromaticity, please draw it. Me B- Me Ме O,N. 2- Br CI MeA) 1) One of the following four structural formulas is not a permissible resonance contributor which one? Why? O HC €0.00 "SEO • HE a) b) NFO NFO HC H.C HC HC 2) Using curved arrows, show the electron movement that connects the three resonance contributors. B) Write the most stable enol forms of the following compound, and choose which of them is more stable With explanation. CH3 لوج شركة اللهDraw the starting materials and mechanism arrows(s) to give the product shown. i Draw the starting materials and mechanism arrow(s). Include lone pairs and formal charges.