Review Topics] References] In eac case below select the synthetic procedure/s that could be used to carry out the transformation, giving the alcohol shown the single major product. The are: Hydroboration/oxidation: alkene + BH3; then H2O2, OH. Oxymercuration: alkene + Hg(OAc)2, H20; then NABH4 CH3 CH3 CH3 CH3 CH3CH2CH2CH=CH2 CH3CH2CH2CH2CH2OH 9 more group attempts remaining Submit Answer Retry Entire Group Previous 08 LO CH3CH2CH2CH=CH2 CH3CH2CH2CH2CH2OH hydroboration/oxidation oxymercuration both methods Submit Answer Retry Entire Group 9 more group attempts remaining neither method Cengage Learning | Cengage Technical Support DD F7 1\ 000 F8 F4 F5 & 5 7. 4.

Provide an IUPAC name for each of the compounds shown. (Specify (E) (Z) stereochemistry, if relevant, for straight chain alkenes only. Pay attention to commas, dashes, etc.) CH3 CH3 1.) -CH2CH3 CH2CH3 2.)

1) alkene (1 mole) 03 (1 mole) 2) (CH3)2S (1 mole) Scheme Q1a Products 1A and 1B? + (CH3)2S=O c) Assuming that in step 2 in the above reaction H2O2 (hydrogen peroxide) is used instead of (CH3)2S (dimethylsulfide), what would be the resulting products 1C and 1D? Draw their structure and circle and name the functional groups in the products.

Please help

Select the best pair of answer below justifying the reason for your choice.

Draw structural formulas for all alkenes that could be used to prepare the alcohol shown below by oxymercuration.

Need help on both of these please.

Provide the principle organic product(s) for the following reactions.  If more than one product is expected, indicate the major one.  Include stereochemistry as appropriate.

$ [References] H₂O + CO₂ + Nal CH₂ HỌC CHO a = Proton transfer d E1 Elimination - f SN1 Nucleophilic substitution = b = Lewis acid/base e E2 Elimination g = SN2 Nucleophilic substitution c = Electrophilic addition The rections above involve synthesis or reactions of alcohols and ethers. Identify the mechanism by which they proceed from among the mechanisms listed. Use the letters a - g for your answers. 1. 2. Submit Answer Retry Entire Group 9 more group attempts remaining Previous Next> Save and Exit Cengage Learning Cengage Technical Support PrtScn F6 F7 1. 2. O F4 % 5 T OH you. ♫ F5 ^ 6 Y H 1₂ H₂O NaHCO3 & 7 [Review Topics] into * 8 CH₂ H₂CH₂ CH₂ I F8 K + 73°F Sunny Home 9 O F9 L ) End 0 8:14 AM □ 6/20/2022 PgDn E = P P B F10 PgUp 4x F11 F12 Ins

Predict the organic products of the reaction. Show stereochemistry clearly. Draw the products according to the specified (R) or (S) designation for each stereocenter carbon atom. H 1) OsO4, pyridine 2) Na,SO3 or NaHSO; in H, O organic products