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- For the following compound, indicate the ring carbon(s) that is/are nitrated when the compound is treated with HNO3/H2SO4: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
- How many alkene products, including E, Z isomers, might be obtained by dehydration of 3-methyl-3-hexanol with aqueous sulfric acid?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 H3CProvide 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 aboveRank 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.What is the major product formed by the monobromination of methylcyclobutane?