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- See image belowShow how the enamine below can be synthesized. Then draw the resonance structure(s) for the enamine. 그20:33 1 : ●●● all the proper notations for depicting resonance. 4. Provide the full mechanism (curved arrows and intermediates) that leads to the product in the scheme below. Draw the structure of the product to help you see how the starting materials will combine. Use that as a clue to figure out how to draw the mechanism arrows. ccare in your scheme. Be sure to use NaOEt 00 i 5. Provide the major organic product of the reaction shown. Determine if these conditions are best for SN2, SN1, E2, or E1. Be sure to indicate stereochemistry by using the proper wedges/dashes in the product. acetone phenyl butanoate Send a chat O
- An electrostatic potential map of boron trifluoride is shown. Is BF3 likely to be a ucleophile or an electrophile? Draw a Lewis structure for BF3, and explain your answer. BF3Please don't provide handwriting solutionWhich nitrogen atom in the structure below is most nucleophilic? Please explain by discussing the electron density around each nitrogen atom. Show at least three resonance structures of the compound. N.
- A. Draw all significant resonance structures of each compound below, using appropriate arrows, and then indicate the most significant contributor (multiple structures may be equal in significance). Briefly explain your reasoning in each case. O: (a). H-O: (b).Need help solving this, please show your work with the answer!Please don't provide handwriting solution
- Draw the major organic product of the Bronsted acid-base reaction between the compounds shown below. Include all lone pairs and charges as appropriate. Ignore any counterions. HH 1 eq. base H H H oIllustrate the resonance effect of the methoxy group -OCH3, on the structure of the benzene ring. Draw all the oissuvke resonance forms of methoxybenzene, including the hybrid Based on the structures, explain how the presence of the -OCH3 group affects: (i) the reactivity of the benzene ring towards electrophilic attack (ii) the orientation or point of attack of an incoming electrophilic reagent on the benzene ring.please answer in text form and in proper format answer with must explanation , calculation for each part and steps clearly