Question 3 1 points What would be the main product of the lithium aluminum hydride reduction...
What would be the products if a triglyceride was treated with a lithium aluminum hydride? Would it make a good detergent?
2. Predict the product of reaction of this acid (from chrysanthemums) with lithium aluminum hydride. 1. LiAlH4, ether 2. H2O OH 3. Both of the molecules shown below are found in multiple plants. Propose reaction conditions at the arrow to accomplish the following synthesis in a good yield. tubro - OH
1. Compare the use of sodium borohydride versus lithium aluminum hydride in terms of handling and usage. 2. Be able to decide when to use sodium borohydride and when to use lithium aluminum hydride for reducing an aldehyde.
Draw the structure of the major product formed in the reaction of t-butylcyclohexanone and lithium aluminum hydride. Draw the major product formed in the reaction of t-butylcyclohexanone and lithium tri-sec-butylborohydride.
B. The reaction of acetonitrile (CH3CN) with lithium aluminum hydride (LIAIHA) gives the following product after treatment with water: | a) CH OH b) CHÚCHO 6) CH CÓ NHU d) CHÚCH 8) CHỤCHẠNH,
d) Product of part (c) with lithium aluminum hydride; then H,0 (e) Product of part (c) with sod Each of the following reactions has been reported in the chemical literature. structure of the product(s) formed in each case. Write the 21.36 Cl2 CH2Cl2 Cl C&HsCH2SH NaOH, H20 NaOH (c)o water
2. Be able to decide when to use sodium borohydride and when to use lithium aluminum hydride for reducing an aldehyde. 3. If you reduce a compound containing an aldehyde, what qualitative test would you use to determine if the product is good or bad? 4. Draw the mechanism for the reduction of vanillin vanillyl alcohol. Oxidation of an Aldehyde (Vanillin III) 5. Be able to determine the oxidation of carbon in different molecules. 6. Write the mechanism for this...
Consider lithium aluminum hydride (LAH), a reducing agent similar to NaBH, shown below. Would you expect LAH or NaBH, to be a stronger (more nucleophilic) reducing agent? Justify your answer. Consider the source of the nucleophilicity as discussed in the recorded lecture
just the balanced equations for main reaction and side reaction with steps and major / minor products please and thank you can you create a balanced stereoselective mechanism equation for both reactions using the 4tertbutyl starting base equation from the 1st previous image for the primary reactions and side reaction equations on the 2nd previous image. and can you also include any major and minor products please and thank you STEREOSELECTIVE REDUCTION OF 4-tert-BUTYLCYCLOHEXANONE OH 1. NaBH4, EtOH 2. H30+...
QUESTION 1 Reaction of pentanoic acid with thionyl chloride produces compound B followed by addition of two equivalents of ammonia to produce which compound? butanamide ammoniumpentanoic acid pentanamide CN-pentylamine QUESTION 2 Pentanoic acid reacts with lithium aluminum hydride followed by water to produce compound B. Compound B is reacted with phosphorus tribromide to give compound C which is then treated with sodium cyanide to produce compound D. Finally, compound D is reacted with lithium aluminum hydride and water to give...