Draw the structure of an eight-carbon alkene that would yield the following compound (and no others) after treatment with ozone followed by dimethyl sulfide. CH3 click to edit
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- Draw the structure of an eight‑carbon alkene that would yield the following compound (and no others) after treatment with ozone followed by dimethyl sulfide. draw the starting alkeneDraw structural formulas for all alkenes that could be used to prepare the alcohol shown below by oxymercurationAn alkene is treated with ozone in presence of zn and acidic aqueous medium. A ketone (2-butanone) and an aldehyde (butanal) is produced. Identify, which of the following alkene is the starting material. options: 5-methyl-2-heptene 3-methyl-2-heptene 3-methyl-3-heptene 4-methyl-2-heptene 5-methyl-3-heptene
- For compound D to E, what is the reaction of a primary alcohol to an aldehyde and what can be the potential reagent? (reduction / oxidation / elimination / substitution) (mCPBA / PCC / CrO3 / LiALH4 with hydronium quench)complete the conversion using SN1, SN2, E1, or E2. what is a possible reagent? cyclohexane --> cyclodi-1, 3- eneConsider a reaction where cis-but-2-ene is treated with OsO4 followed by NaHSO3/H2O. Draw the structure of one product that is formed in the reaction, including correct stereochemistry.
- Draw the constitutional isomer formed when the following alkenes are treated with each set of reagents: [1] H2O, H2SO4; or [2] BH3 followed by H2O2, −OH.Below is a mechanism that represents the following single reaction sequence: a certain alcohol undergoes acid- catalyzed dehydration (conversion that involves the loss of water from the reacting molecule or ion) to form an alkene product. Write the IUPAC name of the product. Include E/Z stereochemistry. Hint: Name of the substituent of the product is similar to that of reactant.Consider a reaction where cis-but-2-ene is treated with a peroxy acid followed by OH- /H20. Draw the structure of one product that is formed in the reaction, including correct stereochemistry.
- A. the products formed when an alkene reacts with these reagents: (i) H2 in the presence of Pd catalyst (ii) HClHow many alkene products, including E, Z isomers, might be obtained by dehydration of 3-methyl-3-hexanol with aqueous sulfric acid?Starting from bromoethane, the formation of which of the following compound requires more than one step of reaction? 2 (a) Methoxyethane (b) Ethanol (c) Ethanoic acid (d) Ethene