H₂O N(CH3)2 H₂SO a. Draw the structure of the tetrahedral intermediate INITIALLY-FORMED in the reaction shown. ☐ You do not have to consider stereochemistry. Do not include counter-ions, e.g., Na+, I, in your answer. In cases where there is more than one answer, just draw one. ChemDoodle b. Draw the structures of the organic products of the acyl transfer reaction.
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- Draw the most stable resonance form for the intermediate in the following electrophilic substitution reaction. (please show which structure I need to put as the answer).Draw the structure(s) for the major final product(s) formed in the following reaction sequence. CN s༠༣ Cl, FeCl. 3 H,SO Click and drag to start drawing a structure. lo 用 8 iYB & {EE□Draw the structure of the major organic product(s) of the reaction. OH • CH,OH NaOCH - You do not have to consider stereochemistry. . All carboxyl and amino groups should be drawn in the neutral form. • If no reaction occurs, draw the organic starting material. - 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.
- Draw the structure of the major organic product(s) of the reaction. NaOH H20 CH3 • You do not have to consider stereochemistry. • All carboxyl and amino groups should be drawn in the neutral form. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in t Separate multiple products using the + sign from the drop-down menu. opy aste Cherr DbodleOrganic Functional Groups Predicting the reactants or products of ester hydrolysis Predict the products of this organic reaction: 0 CH—C—0—CH, H C-CH3 + H₂O Specifically, in the drawing area below draw the condensed structure of the product, or prod in any arrangement you like, so long as they aren't touching.) If there aren't any products because this reaction won't happen, check the No reaction box unPlease don't provide handwriting solution
- Draw the most stable resonance form for the intermediate in the following electrophilic substitution reaction. You do not have to consider stereochemistry. Include all valence lone pairs in your answer.Draw the structure(s) of the major organic product(s) of the following reaction. 1. Dry Et₂O + CH3Mgl H 2. aqueous HCI at 0° • You do not have to consider stereochemistry. • 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. + √n [ ? ChemDoodlePredict the products of this organic reaction: CH3 O || CH3 CH–C−NH—CH3 + NaOH A No Reaction ? Specifically, in the drawing area below draw the structure of the product, or products, of this reaction. If there's more than one product, draw them in any arrangement you like, so long as they aren't touching. If there aren't any products because this reaction won't happen, check the No reaction box under the drawing area. Click anywhere to draw the first atom of your structure. X :0 Ć
- Draw the structure of the major organic product(s) of the reaction. H3C ● `N H 1. LIAIH4, ether FO 2. H₂O • You do not have to consider stereochemistry. • 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.Predict the products of this organic reaction: Specifically, in the drawing area below draw the structure of the product, or products, of this reaction. If there's more than one product, draw them in any arrangement you like, so long as they aren't touching. If there aren't any products because this reaction won't happen, check the No reaction box under the drawing area.d) During the reaction between 3, 3-dimethylbutene (W) and HBr, intermediate species and Y are formed. CH3 CH;-C-CH=CH2 ČH3 HBr Y step 1 step 2 step 3 i) Write a mechanism for the formation of intermediate X? ii) Write the structure of intermediate Y? iii) Explain in your own words what happens in step 2 of the reaction? iv) Write a mechanism for the formation of Z from Y?