Br OH H₂O HO (14 pts) Provide a complete mechanism for the reaction in the box. Include all electron-pushing arrows, lone pairs, and formal charges. HO blo NO (S)
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- what is missing to comprete the tho reactian patnuay below? HO 1) OH 2)Chemistry HO -OEt HCI (catalytic) H₂O + EtOH Draw the arc arrow mechanism. Include all relevant free electron pairs, arc arrows, formal charges, structures of intermediates and by-products. Hint: the reaction starts with the protonation of alcoholConsider the following structures: CH, CH3 H;C, „NH3 H,C, CH H3C, Br H3C. CH CH3 CH3 CH3 JECE CEEJ JEEC СЕЈЕ ЕСЕ Which is a resonance contributor? ECJE Which has a net formal charge of +1? JECE Which has only one type of hydrogen? ECJE Which will form the most stable free radical? JEEC Which is an electrophile? JEEC
- 5. Using curved arrows show the mechanism for the hydrohalogenation for the following reaction. Show how the two possible intermediate products are formed and explain why only one product proceeds to form the product. Clearly indicate attack of electrons and full and partial (8) charges. H-Br Br H-Br Product Intermediate ProductsOEt `H HH ö:Draw curved arrows to indicate the movement of electrons in the following reaction. H H HỌ: Arrow-pushing Instructions HỌ: NOC XT H H---- H H C-CI 1 H CI / HO-C- A HO-C H H H H :CI: :CI:
- 4-44 Draw the important resonance forms of the following free radicals. (a) CH₂=CH-CH₂ (b) (d) (e) -CH₂ (c) (f) CH₂-C-0.Organic Chemistry Мaxwell presented by Macmillan Learning For the dehydrohalogenation (E2) reaction shown, draw the major organic product. Select Draw Rings More Erase H CH;CH2OK CH3CH2OH heat BrDraw the mechanism using curved arrows to show how the electron pairs move for the second step of the given reaction. Include lone pairs and formal charges (if applicable) on the structures. 2m H 哎 1-04 H + H₂O: "X" + HO: + H H
- For each of the reaction below, draw the curved arrows and lone pairs of electrons to show the mechanism. Predict which side of the reaction will be favoured under equilibrium conditions. Give a brief explanation of your prediction. NーH4. Draw the mechanism that accounts for the formation of the product under the conditions shown. You may not add any other reagents. Be sure to show: all intermediate structures that occur in the course of the mechanism, any important resonance structures that play a role in the process, what if anything is added or lost in each step, and all formal charges on the structures. CHO H+ HO-C-H HO OH H-C-OH CH,OH НО 1 2 = 3SEE MORE QUESTIONS