Write the balanced equations (A reduction and a hydrolysis) for the synthesis of sulcatol from 6-methyl-5-hepten-2-one reacting with NaBH4 followed by the addition of H+ and H2O. Use a 3:1 ratio of ketone to NaBH4
Write the balanced equations (A reduction and a hydrolysis) for the synthesis of sulcatol from 6-methyl-5-hepten-2-one...
QUESTION 19 What is the IUPAC name of the following compound? (E)-3-methyll-4-hepten-3-one (Z)-4-methyl-4-hepten-3-one (2)-4-methyl-3-hepten-5-one (E)-4-methyl-3-hepten-5-one QUESTION 20 What is the product of the following reaction after the final acidic workup step? some all answers.
Draw the structures of 6−methyl−5−hepten−3−one and 6,10−dimethyl−5,9−undecadiene−2−one
Please help? Write the balanced chemical equations of: 1) SYNTHESIS OF MERCURY TETRATHIOCYANATOCOBALTATE (II) 2)SYNTHESIS OF TRIS(ETHLYENEDIAMINE)NICKEL(II) THIOSULFATE 3) SYNTHESIS OF DICHLOROBIS(TRIPHENYLPHOSPHINE)NICKEL(II) 4)SYNTHESIS OF PENTAAMMINECHLORIDOCOBALT(III) CHLORIDE 5)SYNTHESIS OF NITROPENTAMMINECOBALT(III) CHLORIDE
OCH3 OH from One route to the synthesis of HO and CH,CH2MgBr is to 1) protect the ketone as an acetal, 2) reduce the ester to an alcohol, 3) hydrolyze the acetal back to the ketone, 4) protect the alcohol as a TMS ether, 5) react the ketone with the Grignard reagent followed by acidic workup to give the desired product. A second route to the desired product would start with the selective reduction of only the ketone to an...
5. propose an efficient synthesis plan for each of the following reactions. 6.Before moving on to N-nucleophiles, let’s check your memory on some ketone reactions. 5. Now, straight from our textbook, propose an efficient synthesis plan for each of the following reactions. ره ماه را OH و . Ph Ah 6. Before moving on to N-nucleophiles, let's check your memory on some ketone reactions. 1. PhMgBr 2. H30* NaBH4, EtOH 1. LAH 2. H2O Zn(Hg), HCI
1. Write the chemical equation for the saponification of methyl salicylate in 6-M NaOH. 2. Write the chemical equation for the hydrolysis of methyl salicylate in 6-M HCI 3. Write the chemical equations for the four esterification reactions a- Acetic acid Benzyl alcohol b- Acetic acid+ isopentyl alcohol c- Acetic acid Ethyl alcohol d- Salicylic acid Methyl alcohol e- Cinnamic acidMethyl alcohol
The balanced redox reactions for the sequential reduction of vanadium are given below. reduction from +5 to +4: 2 VO2+(aq) + 4 H +(aq) + Zn(s) → 2 VO2+(aq) + Zn2+(aq) + 2 H2O(l) reduction from +4 to +3: 2 VO2+(aq) + Zn(s) + 4 H +(aq) → 2 V3+(aq) + Zn2+(aq) + 2 H2O(l) reduction from +3 to +2: 2 V3+(aq) + Zn(s) → 2 V2+(aq) + Zn2+(aq) If you had 14.6 mL of a 0.0033 M solution of...
1. Write equations for the reaction of 2-methyl propane-1- magnesium bromide with acetaldehyde include the hydrolysis of the reaction mixture with dilute acid. B) Why should anhydrous diethyl ether be used rather than regular solvent grade diethyl ether to prepare the solution of benzaldehyde that is added to the Grignard reagent, 2- methyl propane-1- magnesium bromide? C) By drawing the structure indicate the polarity (charge separation) of the bond between carbon and bromine in 1-bromo-2-methyl propane. Is 1-bromo-2-methyl propane electrophile...
The balanced redox reactions for the sequential reduction of vanadium are given below. reduction from +5 to +4: 2 VO2+(aq) + 4 H +(aq) + Zn(s) → 2 VO2+(aq) + Zn2+(aq) + 2 H2O(l) reduction from +4 to +3: 2 VO2+(aq) + Zn(s) + 4 H +(aq) → 2 V3+(aq) + Zn2+(aq) + 2 H2O(l) reduction from +3 to +2: 2 V3+(aq) + Zn(s) → 2 V2+(aq) + Zn2+(aq) If you had 11.8 mL of a 0.0031 M solution of...
Design a synthesis of (Z) 5-methyl-2-hexene from propyne and 2-methyl-1-propanol. H -CH3 and OH Part 1 Choose the best option for the immediate precursor to (Z) 5-methyl-2-hexene. CH Br Br This alkyne can be converted to (z 5-methyl-2-hexene in one step. Part 2 out of 9 Choose the best option for the nucleophile precursor to 5-methyl-2-hexyne. CH3