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- The hydrolysis of CH3-CH=CH-CH2-Cl gives rise to two products: CH3-CH=CH-CH2-OHl and CH3-CH(-OH)CH=CH2. Write a mechanism that accounts for their formation. Show each step clearly. Use curved arrow notation.What are the following alkenes, E or Z? if neither label as such as with bothBased on the hydrogenation reaction information, how many different alkene structures can you draw that could be Compound X? (If enantiomers are possible, count each pair of enantiomers as one structure.)
- In the given alkene below, what is the configuration of the double bond? Give the letter onlyProvide an IUPAC name for the compound below. ball & stick 0O labels (Specify (E) or (Z) stereochemistry, if relevant, for straight chain alkenes only. It is not necessary to use italics in writing compound names. Pay attention to commas, dashes, and parentheses. )Draw the bond-line (skeletal) structure of the compound with molecular formula C₂H₁3Br that gives the following alkene as the exclusive product of E2 elimination. Click and drag to start drawing a structure. C X C Ś c+
- Based on the hydrogenation and the bromination reaction information, how many different alkene structures can you draw that could be Compound X? (If enantiomers are possible, count each pair of enantiomers as one structure.)4) Draw the complete electron-pushing arrow mechanism for the following reductions. Explain, using resonance contributors, the regiochemistry that results in each case. ỌMe Na, MeOH ? NH3 CHO Na, MeOH ? NH3Provide an IUPAC name for each of the compounds shown. (Specify (E)/(Z) stereochemistry, if relevant, for straight chain alkenes only. Pay attention to commas, dashes, etc.)
- 6) Develop a series of reactions we have covered in lecture that would produce the following molecules. Use any reagents necessary, but you must start with an alkene with one double bond (any alkene you choose) as one of your reactants. онI 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.Based on the images attached, choose the alkene product formed for the following reaction and predict the major and minor compounds.