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- Draw the major organic product(s) of the following reactions including stereochemistry when it is appropriate. CH3-CEC-CH3 ● H₂O/H₂SO4/Hg+² • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • If no reaction occurs, draw the organic starting material. Separate multiple products using the + sign from the drop-down menu.Curved arrows are used to illustrate the flow of electrons. Follow the arrows and draw the intermediate and product in this reaction. Include all lone pairs. Ignore stereochemistry. Ignore inorganic byproducts. H-O :OCH₂ CH₂OH₂* :0: protonation Draw Intermediate CH3OH₂+ protonation CH3OH deprotonation loss of H₂O elimination 1 H₂C CH₂OH nucleophilic addition O-H Draw Intermediate CH3OH n deprotonatio Draw ProductDraw the major organic product(s) of the following reactions including stereochemistry when it is appropriate. H₂O/H₂SO4/Hg+2 CH3-CEC-CH3 • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • If no reaction occurs, draw the organic starting material. Separate multiple products using the + sign from the drop-down menu.
- Indicate the product obtained by reacting A and B. A || H3C-S-CH₂ Na* || CH 3 B CH2. C. CH3 H3C CH3Classify attached carbocation as 1°, 2°, or 3°.Draw the major organic product(s) of the following reactions including stereochemistry when it is appropriate. H,O/H,SO, / Hg*2 CH3-CEC-H • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • If no reaction occurs, draw the organic starting material. • Separate multiple products using the + sign from the drop-down menu.
- Identify the alcohol reactant needed to produce each of the following compounds as the major product of an alcohol dehydration reaction. H,SO, Alcohol → CH3–CH=CH–CH3 180°C a. H,SO, Alcohol → CH,=CH-CH–CH3 180°C CH3 b. H,SO, Alcohol CH3-CH-CH2–0–CH,-CH–CH3 140°C ČH3 с. H,SO, Alcohol CH,=CH-CH,–CH3 180°C H,SO, Alcohol CH;-C=C-CH3 180°C CH3 CH3 e.12) Use the curved arrow formalism to show the movement of electron pairs in the following reaction and label each reactant as a nucleophile or an electrophile. CHÍNH CHỊCH, + CO Học Nha CH₂CH₂CIDraw a structural formula(s) for the major organic product(s) of the following reaction. Br + CH3CH₂O™ Na* ethanol • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • You do not have to explicitly draw H atoms. • If a group is achiral, do not use wedged or hashed bonds on it. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate multiple products using the + sign from the drop-down menu.
- 1) identify the reactant/s in the chemical equation and circle it, also name its major functional group 2) identify the product/s in the chemical equation (circle it) and name its functional group 3) is the a reversible reaction or not? How do we knowFor each reaction in question 20, sketch a reaction coordinate energy diagram indicating the starting materials, transition states and any intermediates, if present, in the reaction. Don't worry about the absolute energy of starting materials and products but you can assume that the product is more stable than the starting materials.* Question Completion Status: 1 2 3 4 QUESTION 7 5 Which substituent will have the highest A value (AG for inverting a chair with the subsituent). OA-2,2-dimethylbutyl (aka)neo-pentyl OB 1,1-dimethylpropyl (aka tert-pentyl) OC3-methylbutyl (aka isopentyl) OD1-ethyl-1,1-dimethylsilyl 0000 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 QUESTION 8 Which compound is aromatic? OA