Predict the product(s) and provide a full arrow-pushing mechanism for the reaction of 4-methyl-1-hexyne with two equivalents of hydrobromic acid.
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Predict the product(s) and provide a full arrow-pushing mechanism for the reaction of
4-methyl-1-hexyne with two equivalents of hydrobromic acid. If necessary, label major
and minor products.
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- Provide the mechansim using curved arrows of the reaction of p-t-butyl phenol treated with acetic anhydride in AlCl3. Include resonance stabilized intermediates and if more than one product is formed, label them as major, minor, etc. thank you for the helpPropose a detailed mechanism for the reaction below (in the attached picture), showing the structure of thestable intermediate and using curved arrows to indicate electron flow in each stepIn the presence of acid such as H2SO4, 3,4-dimethyl-1-pentene undergoes isomerization to 2,3-dimethyl-2-pentene (shown below). Write a complete mechanism, showing all steps and using curved arrows to explain this observation.
- Predict the major product for the following reaction and give the complete arrow pushing mechanism to show the formation of the product.Propose a mechanism for the acid-catalyzed hydration of propene. Remember that a mechanism must include curved arrows to show movement of electrons, as well as all intermediates.Draw structural formulas for the major product(s) formed by reaction of 3-hexyne with each of these reagents. (Where you predict no reaction, write NR.) Q.) H2O in H2SO4/HgSO4
- Draw structural formulas for the major product(s) formed by reaction of 3-hexyne with each of these reagents. (Where you predict no reaction, write NR.) Q.) H2/Lindlar catalystFor the following question please: 1. Predict the products: 2. Give the correct mechanism via correct arrow pushing, and arrow formalisms: 3. Name each mechanism 4. Name each MAJOR and MINOR products: (1R, 2S)-1-iodo-2-methylcyclohexane + KN3 /DMFComplete the following mechanism for the acid-catalyzed rearrangement of 1-vinyl-2-phenylcyclopropane to give both isomers (E / Z) of 5-bromo-5-phenyl-2-pentene employing the curved-arrow/arrow-pushing formalism.
- -Reactions E1 and E2 with AlcoholsIt develops the following reaction mechanisms and the main and secondary products:Fill in the missing reagent/product(s) for the following reactions.(a) Propose a mechanism for the conversion of cis-hex-3-ene to the epoxide (3,4-epoxyhexane)and the ring-opening reaction to give the glycol, hexane-3,4-diol. In your mechanism, payparticular attention to the stereochemistry of the intermediates and products.(b) Repeat part (a) for trans-hex-3-ene. Compare the products obtained from cis- andtrans-hex-3-ene. Is this reaction sequence stereospecific?