5. Predict the major product obtained when the following compound is treated with Birch conditions: Write down the detail mechanism for the product formation. I Na, CH₂OH NH₂
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- Compound A on ozonolysis yields the two products shown. What is the structure of compound A? Compound A 1.03 2. (CH3)2S ||| ol H H || IV H HGive the major organic product of the following reaction. 1) ВН3/THF 2) NaOH, H2O2 HO OH HO- OH There is no reaction under these conditions or the correct product is not listed here.Draw the major organic product obtained by reaction of benzoyl chloride with dimethylamine, (CH3)2NH.
- Predict the product of the following reaction. A OH HNO3, H2SO4 B Name the organic product without stereochemistry. What is the molecular formula of the product?Draw a structural formula for the product that forms when the following compound is treated with K,Cr,O7. он K2Cr207 CH;CHCH3 H2S04 • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. opy aste - [F CH ChemDoodleH3C N- H₂NNH₂ H⭑ CH3 H3C IN CH3 Hydrazine reacts with 2,4-pentanedione to yield 3,5-dimethylpyrazole. Including protonations and deprotonations, the reaction takes 12 steps. Write out the mechanism on a sheet of paper and then draw the structure of the product of step 6. • You do not have to consider stereochemistry. •You do not have to explicitly draw H atoms. • Do not include lone pairs in your answer. They will not be considered in the grading. • In an elimination step, include the structure of the leaving group, but draw it in its own sketcher. Separate structures with + signs from the drop-down menu. ? Sn th Previous Next
- Birch Reduction of toluene leads to a product, X with the molecular formula C7H10. After ozonolysis of X, the two compounds, 3-oxobutanal and malonaldehyde are formed. what is the structure of xThe hemiacetal reaction is also reversible and can also be catalyzed by either acid or base. Hemiacetals are not usually isolated, except in the formation of 5- and 6-membered rings, as often seen in carbohydrate chemistry. Identify the hemiacetal formed from the intramolecular cyclization of the molecule shown. OH OH NaOH ? H CH₂OH OH OH The hemiacetal product is: HOH₂C HO O HOH₂C H OH OH HO OH HO OH HO OH O HOH₂C О OH OH H HO- OH HO OH CH₂OH OH OHProvide all the reagents and show all structures of the product formed in each step, not just a list of reagents. b) Benzene c) Toluene OHC Ĵ Ĉ COOH
- Predict the product (including stereochemistry) when the following substance reacts under thermal conditions. H H3C- H3C- H.What is the major product formed when 3-methyl-1-butene is treated with Hg(C2H3O2)2 in a THF/ethanol mixture followed by NaBH4 in base?Give IUPAC names for the following structures. If appropriate, specify relative stereochemistry. نما OH 1st structure: 2nd structure: S SCH3 SCH3