1) Draw the product and mechanism for this transformation. Use electron-movement File Preview se the back if insufficient room. (9 pts). H+ Q= NH2 'N' H - NH 3
Q: The answers are not 1.77E-9 and 1.55E-5. Please help.
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Q: For the first one, I've also tried 1.7E-9 and 1.77E-9. Neither is correct.
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- Determine the mechanism of nucleophilic substitution of each reaction and draw the products, including stereochemistr CH₂CH3 CI Br + CN d. + CH3COOH a. acetone + -OCH3 e. DMF f. b. C. ||||| a ||||| Br H Br CH2CH2CH3 + CH3OH DMSO H CH3 CI Br + OCH₂CH3 + CH3CH₂OHDraw a stepwise mechanism for the following acid-catalyzed addion of water H X÷X H₂O Part 1: view structure Part 2: Part 3 out of 4 5 attempts left H 0 view structure F X 6° view structure edit structure... Check my work + F F H30+ F™ HO™ H₂O HF X₂ view structure CH f CH H edit structure H TE OH Next part OH e9 Draw an arrow-pushing mechanism for the acetal below. at O + HO OH excess H* ← (6) Draw the resulting product of the reaction if there had been HD- instead of Ht Explain why the products in a and b are different.. Why are acetals / Ketals used as protecting groups for aldehydes | Ketones.
- Please draw an arrow pushing mechanism of this reactionWhich reagent is the nucleophile in the esterification reaction shown below? O || С-ОН Benzoic Acid methanol methyl benzoate benzoic acid sulfuric acid + CH₂-OH Methanol H₂SO - H₂O O || C-O-CH3 Methyl benzoateBe sure to answer all parts. Draw a stepwise mechanism for the following reaction: Part 1 out of 3 0=0 finish structure ... 10 attempts left &=d OH H₂SO4 T draw structure ... Check my work H₂SO4 HO™ HSO4 H3O* Next part
- b Use curved arrows to show the mechanism of the step below. If more than one resonance form of the product is possible, show the most stable form. Arrow-pushing Instructions ^^C↔X™ H to HI.... H3CDraw the mechanism of A and B reactions below using appropriate reagents.Q6. Propose a mechanism for the following reaction: Br CH3O + Br
