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- Please correct answer and don't use hand ratingThis problem is too complicated to type out, so I attached a picture of the problem.Two students are given the starting material benzoic acid and are asked to prepare benzaldehyde. The first student starts by refluxing her sample of benzoic acid in thionyl chloride in the fume hood. Upon completion of the reaction, she evaporates the thionyl chloride to isolate compound A. She treats compound A with a stoichiometric amount of lithium tri-tert-butoxyaluminum hydride at –78 °C in diethyl ether, producing compound B. Adding water, she isolates her product, compound C. The second student takes a different route. She treats benzoic acid with an excess of lithium aluminum hydride (LAH) in diethyl ether, followed by careful addition of ethyl acetate to remove any unreacted LAH. She adds water and isolates her product, compound D. Draw the structure for compound A, compound C, and compound D. Draw compound A. Draw compound C. Select Draw Rings More Erase Select Draw Rings More Erase // Cl C C
- #5 please answer part d and ePlease don't provide handwrittin solution...The solvent front distance is from ... Group of answer choices the bottom of the paper to the top of where the solvent reached. the baseline to the top of where the solvent reached. from the top of the spot to the top of the paper. the bottom of the paper to the top of the paper. from the top of the spot to the top of where the solvent reached.
- Check the box next to each molecule on the right that has the shape of the model molecule on the left: model 2 3 4 I None of the above 6 17 8 I molecules (check all that apply) 0⁰3 NO3 H₂O* O NH3 X You can drag the slider to rotate the model molecule.Please correct answer and don't used hand raitingCheck the box next to each molecule on the right that has the shape of the model molecule on the left: model 4 I 5 None of the above 6 7 I I 8 I molecules (check all that apply) H₂S H₂O HOCI BrCN X Start over You can drag the slider to rotate the model molecule.
- Please solve correctly with explanation. Thank youQUESTION 2 Consider the line angle for ibuprofen. How many sp3 carbons are present? HO. ibuprofen 4. QUESTION 3 Which functional groun is NOT present on this molecule? Click Save and Submit to save and subrmnit Click Save All Answers to save all ai 6.Rank the following from weakest to strongest intermolecular force. CH3 (a) H3C-C-CH2-CH3 CH3 (b) H3C-CH2-CH2-CH2-CH2-CH3 (c) CH3 H3C-CH-CH3 < Instruction: Please input a, b, or c in each blank.