Which is the more stable form of acetophenone? O Only III Only II I and II are equally stable Only I OH A Moving to another question will save this response. =

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Give the IUPAC name for the followving alcohol. Be sure to answer all parts. Но HO Η H. [Also label the stereogenic centers as R or S.] (2R.3R) (select) (seleet) H3 ol v

10:06 .l LTE chem1 CI CI Compaund A Compaund B a) draw the enantiomers of Compound A and Compound B if possible b) what is the Structeural reationship between compaund A and campaund B? ••. Share Modify Comment More

A A Aav ApE AaBbCcDd AaBbCcDd AaBbCc AaBbCcD AaB x A- . A 11 Normal 1 No Spac. Heading 1 Heading 2 Title nt Paragraph Styles 3. For the following molecule: a. Draw both chair conformations and label substituents as axial or equatorial. b. Indicate which contormation is more stable using equilibrium arrows. equilibrium arrow Frglish (United Statas) 5 & nccessie ty: nvestiuate loxt Preuictions. On to search 99+ アー FIO F11 F12 %23 & 3 4 6 7 R T Y U P D G J |K L V Alt Alt Ctri B LL

11:47 PM Fri Mar 3 ← Select to Draw cat. H2SO4 SO3 (1 equiv) Select to Draw ●●● Problem 49 of 21 Please select a drawing or reagent from the question area 18% Submit

What are the product  Only typed solution

6) What would be the main difference in the IR between the starting materials and the product? A. No C-H stretches in the product B. No C O stretches in the product C. No C-C stretches in the product D. One less C=O stretch in the product than the starting materials Ph Ph + OEt

When gamma-pyrone is treated with the strong acid HBF4, it readily forms a water-soluble salt A, C5H5O2BF4. Draw the most stable resonance structure for A. 1 eq. HBF4 C5H5O₂BF4 A Y-pyrone • Draw cations and anions in separate sketchers. • Separate structures with + signs from the drop-down menu. Sn [F