How many organic products are there in the reaction of 1,3-cyclohexadiene with HBr? (note: be sure to draw out the possibilities before deciding; remember that only the more stable cation is formed) O O three one two four HBr ?
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- Which will be more stable, cis or trans-1,4-tert-butylcyclohexane? Explain by drawing their structures?The substitution reaction below forms two ehters (which are consitutional isomers). Please draw the structures of the 2 ethers formed. Are the ethers single enantiomers or racemic mixtures?2)Major organic products? please write them both in their systematic IUPAC Please answer very soon will give rating surely
- What is(are) the product(s) in the Pd-catalyzed hydrogenation of 1,2-dimethylcyclopentene? Include stereochemistry.Which of the following statement/s is/are false about the reaction of 3-methylhex-3-ene with H3O+?Please tell the outcome of the addition of HBr to (a) trans-2-pentene, (b) 2-methyl-2-butene, and (c) 4-methylcyclohexene. Also please list how many isomers can be formed in each case.
- a. Identify two alkenes that react with HBr to form 1-bromo-1-methylcyclohexane without undergoing a carbocation rearrangement. b. Would both alkenes form the same alkyl halide if DBr were used instead of HBr? (D is an isotope of H, so D+ reacts like H+.)In the given alkene below, what is the configuration of the double bond? Write the letter only.The heat of hydrogenation of cis-2,2,5,5-tetramethyl-3-hexene is -154 kJ (-36.7 kcal)/ mol, while that of the trans isomer is only -113 kJ (-26.9 kcal)/mol. Q.) Why is the heat of hydrogenation of the cis isomer so much larger (more negative) than that of the trans isomer?
- 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.)Write the monobromination products of 1,4-dimethylcyclohexane and calculate the percentages of each product. Which is the major product?Draw the structure(s) of all of the alkene isomers, C5H10, that contain a branched chain. Consider E/Z stereochemistry of alkenes.