Br H3C CH3 a b с ionization d 1-propanol e Prelab Question #4 Homework Unanswered H H 8+ With respect to the mechanism in Scheme 3, which of the following is/are correct? + 1-propanol is a polar aprotic solvent CH3 tertiary carbocation bromide is a poor leaving group both B & D CH3 Select an answer and submit. For keyboard navigation, use the up/down arrow keys to select an answer. K potassium tert-propoxide is reacting with an electron-deficient proton tert-butyl bromide is undergoing an SN2 reaction CH3 Scheme 3. Mechanism of an E1 reaction. H H CH3 CH3 2-methyl-1-butene + CH3 propanol

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Quèstion 2 Predict the major product for the following reaction Br2/AIBR3 CH2 Br -CH2 -Br II Br C-CH2 Br II IV -CH2- Br V

Discussion Prompt #3 CH3 H-Br Br CH3 Draw the mechanism for the reaction above

Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions IXOU H3C Submit Answer H3C Arrow-pushing Instructions CH3 CH3 H-Br CXT H Retry Entire Group Submit Answer CH3 Retry Entire Group H3C H3C 8 more group attempts remaining CH3 + H H CH3 8 more group attempts remaining CH3 Br

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+ k Draw the product of the reaction shown below. Ignore inorganic byproducts. If the reaction results in a mixture of ortho and para isomers, draw only the para-product. 1 Br2 (1 equiv) FeBr3 Drawing U L L U U I I Q

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Draw the arrow pushing mechanisms and product

Predict the major organic product of the reaction of 2-methyl-1-propene or 2-methylprop-1-ene and water in sulfuric acid. Draw the organic product. Select Draw Rings More Erase C H O H CH3 H CH3 + H H H₂SO4 3 Q2 Q