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- Label the following alkenes from most stable, moderate and least stable.Please answer this NEATLY, COMPLETELY, and CORRECTLY for an UPVOTE. What is the most stable carbocation below?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.... H3C
- how do we know which one is carbon 1 ，which one is carbon2？Did I draw the compound correctly？Step by step explain why I know that The stereochemistry of carbon‑1 is S. （but how do you know which one is carbon 1？？？？） The other bromine is attached to carbon‑2？does Br has priority in naming？if so ，dash Br and wedge Br ，which one get priority？why tert tert-butyl-group can’t be Carbon 1 or carbon 2？ The tert‑butyl group is attached to carbon‑4 （base on the picture，why not carbon 3 or carbon 5？？？I am studying so much but I am not sure if these are correct. Can you go over it plsss? A Hoffmann product is O the result of the fastest mechanistic process. the most highly substituted alkene possible. the same as the Zaitsev's product, but the term "Hoffmann" is used for E2. the most stable alkene. What does Zaitsev's rule state? As the degree of substitution around the C=C of an alkene decreases, the stability of alkene increases. None of the statements is correct. O As the degree of substitution around the C=C of an alkene decreases, the stability of alkene decreases. As the degree of substitution around the C=C of an alkene increases, the stability of alkene decreases.5. Which bromocyclohexane starting material would react faster - the cis or trans, and explain why? Draw both chair forms of the starting material to prove your point. Br K* OC(CH) K* OC(CH); Br cis trans
- How do I rank these from best to poorest leaving group? Do I base it in the size of the electronegative atom size?14. What are the differences between ortho-, meta-, and para-nitroaniline? a) Number of substituents on the benzene ring b) Positions of the substituents on the benzene ring c) Position and number of substituents on the benzene ring d) None of theseChoose the answer that most accurately provides the missing starting material; followed by the missing reagent for this reaction. 1. Mg, Et,0 starting material? 2. reagent ? 3. acidic work up (H*) a. benzene; oxirane b. aniline; 1-methyloxirane c. benzene; 2,2-dimethyloxirane d. toluene; 2-ethyloxirane e. toluene; 2,2-dimethyloxirane f. benzene; 2,2-dimethyloxirane