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- How to synthesize trans-2-methylcyclohexanol from cyclohexanone?b) The Wolf-Kishner reduction is a reaction used in Organic Chemistry to convert carbonyl functionalities into methylene group. The reaction was used to convert an aldehyde or ketone to an alkane using hydrazine, base and thermal conditions. The mechanism begins with the attack of hydrazine of the aldehyde or ketone. Stage 1: The reaction of aldehyde/ketone with hydrazine to produce hydrazine Stage 2: Reaction with the base and heat to convert hydrozone to alkane Write the mechanism of the reaction.9. NAHSO3 CH3 - C- CH3 19)_ 10. _(10a) NaOH → HC-O-Na + _(10b)_
- Rank the following compounds in order of increasing basicity. CH3 CH3 O₂N ||| fo H3C CH3 CH3 IV A) || < | < V < III < IV B) || < V < | < ||| < IV C) IV < I< III < V < || D) || < V < ||| < | < |V H3Cplease answer completely from a-eDraw the principal organic product for the reaction of 2-bromohexane with lithium in diethyl ether, followed by formaldehyde in diethyl ether, and then followed by dilute acid. Click and drag to start drawing a structure. X A G P
- 11) Synthesize 2-methyl-3-hydroxycyclohexone from cyclohexone, methyl iodide, and inorganic precursors.(a) Draw the structure of the hemiacetal formed from one mole of benzaldehyde and one mole of ethanol. (b) Draw the structure of the acetal formed from one mole of benzaldehyde and two moles of ethanol. (c) Draw the structure of 2-methoxy-2-butanol. What compounds could you prepare this from? (d) Draw the structure of 3-methoxyl-2-butanol. What functional groups are present? Is this an acetal, a hemiacetal, or neither? Explain. (e) Identify the functional groups in the molecules shown below. Circle any acetals or hemiacetal, and identify which they are. 0-rank these compounds in order of increasing basicity Rank these compounds in order of increasing basicity (most basic at the bottom). C A B G Drag and drop options into correct order and submit. A too B FF |||
- (a) Draw the structure of the hemiacetal formed from one mole of benzaldehyde and one mole of ethanol. (b) Draw the structure of the acetal formed from one mole of benzaldehyde and two moles of ethanol. (c) Draw the structure of 2-methoxy-2-butanol. What compounds could you prepare this from?How would you convert ethanoic acid into benzene?Click on a basic (nucleophilic) atom. HH | | H-C-C=C₂ | H H H H-CI: