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- How many alkene products, including E, Z isomers, might be obtained by dehydration of 3-methyl-3-hexanol with aqueous sulfric acid?Draw the main organic product formed in each of the following reactions:In the boxes provided, give the structure and stereochemistry (when necessary) of the major product(s) formed in the reactions shown. G 1.2 eq. MeMgBr 2. H₂O
- What products are formed when the following compound reacts with ozone and then with dimethyl sulfide?X Upon ozonolysis, Compound X produces two compounds: Compound Y and Compound Z. Compound Y can also be prepared from the following synthetic route: PCC 1. R₂BH, THF 1. Mg. Et₂O PCC Compound Y 2. CH₂Cl₂ 2. NaOH, HO CH₂Cl₂ 3. H₂O* From this information, draw the structures of Compounds X, Y, and Z. For Compounds X and Z, different substituents are possible. For grading purposes, just use hydrogens as the substituents. Br مرد →] ►Which of the given compound is most reactive towards E2 elimination? CI H3C, ICH3 H3C CI H3C CI H3C "CH3 H3C CH3 CI H3C
- Provide the structure of the major products formed in the following reaction sequence. CH₂CH₂CH.CCI AICI: A Zn (Hg) HOI A BWhich of the compounds will undergo a carbocation rearrangement upon heating in CH3CH2OH?What product is produced when ethylene oxide is treated with HBr? a Alkylhalide b Alkene c Halohydrin d none of the above
- What is the major product formed by the monobromination of methylcyclobutane?Rank the following compounds from greatest tendency to least tendency to undergo nucleophilic aromatic substitution: chlorobenzene 1-chloro-2,4-dinitrobenzene p-chloronitrobenzene a. Rank the same compounds from greatest tendency to least tendency to undergo electrophilic aromatic substitution.Two products are possible when pent-2-ene is treated with HBr. Write the structures of the possible products, and explain why they are made in about equal amounts.
