The nucleophilic aromatic substitution reaction of a halobenzene with a strong base (KN(CH3)2 in NH(CH3)2) involves a benzyne intermediate. Complete the mechanism below by providing the missing curved arrow notation, lone pair electrons, and formal charges. Do not add additional structures or counterions. ici. ci ငေး H i i Add the missing curved arrow notation, lone pair electrons, and formal charges to all atoms.
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- Draw a mechanism for the reaction of methylamine with formic acid. In the box to the left, draw any necessary curved arrows. Show the products of the reaction in the box to the right. Include any nonzero formal charges and all lone pairs of electrons. Finally, check the box to indicate which side of the reaction is favored at equilibrium.complete the mechanism for his reaction by adding curved arrows and products. Add steps as necessary, and be sure to include lone Pairs and charges where relevant. Draw a curved arrow mechanism for the substitution reaction that will occur with the alkyl halide and nucleophile below, adding steps as necessary. Be sure to include all nonbonding electrons and all nonzero formal charges, and show all species that react or are formed in this reaction.
- Provide a mechanism including relevant resonance forms, intermediates, reaction arrows, and curved arrows showing electron flow.An NH2 group_____ the ring toward electrophilic aromatic substitution by _____. Answer choices in pictureIn electrophilic aromatic substitution, a group attached to the aromatic ring does not affect ring reactivity. Is that true or false?
- need it with detailed explanation don't copy from other sources I will downvoteWhich of the dompounds is most basic and why?The question is: "Draw the curved arrow mechanism for the reaction between (2S,3S)-3-methylhexan-2-ol and PCl3. Note the specific instructions for each box. Include nonzero formal charges and lone pairs of electrons on all appropriate atoms" I attached screenshots of the picture of the atoms below. What type of reaction (SN1, E1, SN2, or E2) would the reaction be, and how would these molecules interact? The question asks for multiple steps so I am guessing it is either SN1 or E1, but what is the reaction mechanism?
- Complete the curved-arrow mechanism for the scheme below by adding any missing atoms, bonds, charges, nonbonding electrons, and curved arrows.Draw the structure(s) of the major organic product(s) obtained after workup of the following reaction. You do not have to consider stereochemistry. If no reaction occurs, draw the organic starting material. Include counter-ions, e.g., Na+, I-, in your submission, but draw them in their own separate sketcher. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner.Nucleophilic attack may appear to occur in two steps as shown below. The alcohol is the nucleophile in this example. It attacks a carbon with a δ+ charge. The second arrow shows the flow of negative charge. WHY is it necessary? The second arrow could be thought of as a resonance arrow. HOW?