I. ITUPUN L UI TUDO TOHO reagents and any inorganic reagents needed in four steps. (16...
extra credit orgo chem NaBH MOH 1.Write two starting materials (five or fewer C's) that react to form the target molecule starting from any carbonyl compound and any organometallic reagent. OH Part IV. Mechanistic Puzzlers (16 pts) 10. Reduction of cyclohexanone using lithium aluminum hydride gives a deuterated alcohol when D.O is used instead of H.O in the workup step. Account for this outcome with a mechanism, showing curved arrows, the key intermediate, and lone pairs and charges. (6 pts)...
Synthesize this from 4 carbon or less alcohols and any organic or inorganic reagents needed and any inorganic compounds. Include all mechanisms, steps, reagents, and reactions used. СН3 NH2 СН3
Synthesize this from 4 carbon or less alcohols and any organic or inorganic reagents needed and any inorganic compounds. Include all mechanisms, steps, reagents, and reactions used. CH3 NH2 СН3
Starting with Benzene and any alkyl halide with four or fewer carbons and any needed inorganic reagents, show how you would synthesize the following compounds: a)m-bromoiodobenze b) m-chloroethylbenzene c)o-nitroalinine d) m-hydoxybenzoic acid e) p-methylbenzonitrile
Synthesis with 10 steps or less Synthesis Problem Show all the steps required, including intermediates, for the synthesis of the following target compound, using any starting material with six (6) carbons or less, plus any other organic or inorganic reagents necessary. Determine the IUPAC systematic chemical name for your target compound. Try for io sieps or tesvs Synthesis Problem Show all the steps required, including intermediates, for the synthesis of the following target compound, using any starting material with six...
Starting with nitrobenzene (PhNO2) and using any other inorganic reagents, synthesize phenol (PhOH). Show the conditions and major organic product for each step.
4. Synthesis. You may use benzene (that is the starting material for a), any organic reagents that contribute four or fewer carbon atoms to the final product, and any inorganic reagents OH OH HN NH 4. Synthesis. You may use benzene (that is the starting material for a), any organic reagents that contribute four or fewer carbon atoms to the final product, and any inorganic reagents OH OH HN NH
Name: 4. Starting with benzene and any inorganic or organic reagents, outline all steps in the synthesis of the following compounds. No mechanisms required but correct order is. (HINT: think clectrophilic aromatic substitution) (10 points): (A) (B)
Name: 4. Starting with benzene and any inorganic or organic reagents, outline all steps in the synthesis of the following compounds. No mechanisms required but correct order is. (HINT: think clectrophilic aromatic substitution) (10 points): (A) (B)
VI. Starting from acetylene (CH C H) and using any needed reagents to synthesize the following molecule: Show every single step of the synthesis (10 pts)