Draw the simplest curved arrow mechanism possible for the reaction shown below. You may need to re-draw structures to show bond lines or lone pairs. 무 × G : ☐
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- Draw the simplest curved arrow mechanism possible for the reaction shown below. You may need to re-draw structures to show bond lines or lone pairs. + YX 右 X > 口 ух2 × G + Draw the simplest curved arrow mechanism possible for the reaction shown below. You may need to re-draw structures to show bond lines or lone pairs.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.
- Draw the simplest mechanism possible for the reaction below. You may need to re-draw structures to show bond lines or lone pairs. Note to advanced students: There may be more than one resonance structure for one of your products. Make sure the mechanism you draw creates the resonance structure that's shown. 9 ( X : G + H,O но ? + H₂O RKetones and aldehydes are hydrated under acidic or basic conditions. An example of the acid-catalyzed hydration is shown. Complete the first step of this mechanism. Include all lone pairs of electrons, curved arrows, and nonzero formal charges in your mechanism.Write the systematic name of each organic molecule: structure ОН но но ОН ОН ОН ОН ОН name М О
- Draw the simplest mechanism possible for the reaction below. You may need to re-draw structures to show bond lines or lone pairs. Note to advanced students: There may be more than one resonance structure for one of your products. Make sure the mechanism you draw creates the resonance structure that's shown. བྱི “དབྱིན 1:| ཐ ད ན “ 1 ཀྱིས .CN + CN + ח'Draw a resonance structure, complete with all formal charges and lone (unshared) electron pairs, that shows the resonance interaction of the acetoxy with the para position in phenyl acetate. phenyl acetate ● CH3 • You do not have to consider stereochemistry. • Include all valence lone pairs in your answer. In cases where there is more than one answer, just draw one. Sn [F ?Ketones and aldehydes are hydrated under acidic or basic conditions. An example of the acid-catalyzed hydration is shown. Complete the first step of this mechanism. Include all lone pairs of electrons, curved arrows, and nonzero formal charges in your mechanism.
- Explain why the following reaction takes place as shown. Be sure to fully explain why the reaction sites are used and what is happening to the formal charges. Include a possible explanation for the negatively charged oxygen reacting with the carbon bonded to the CI rather than the carbon bonded to the SH. SH -- د SHComplete the following acid-base reaction . Show all valence electrons on the interacting atoms and show by the use of curved arrows the flow of electrons in each reaction.осх (Intermediate) Reactant ķ H H: Tip: Only add curved arrows in this sketcher 1
