1) Provide the R/S and D/L designation for the following enantiomers: H H E H- OH HO -H CH OH CH OH 2) Draw all non-hydrogen substituents in the equatorial position for the following compound: H H OH HO -H H- OH HOHC -H OH 3) Is the structure you drew in question No. 2 above a or a anomer? 4) What is the reagent that allows you to form the methyl ether analog from compound you drew in No. 2? 5) Draw a six membered ring lactone and lactam and show the hydrogen bonding between these two molecules. 6) Fill in the missing boxes below: SOCl2 HN 7) Draw the final product for each reaction below: LAH HO DIBAL-H MeMgBr or MeLi 8) Fill in the missing boxes below: -OH HI 1) LDA 2) Br OE 11 9) Could you have used NaOEt instead of LDA and obtained the same final compound? 10) Synthesize the following compound from any reagents and building blocks 2 carbons or less. . ala