What amide would you react with LiAlH4 to form benzylmethylamine. Show mechanism.
What amide would you react with LiAlH4 to form benzylmethylamine. Show mechanism.
Draw the mechanism for the acid-catalyzed reaction of an amide with a methanol to form an ester. Draw the mechanism for the acid-catalyzed reaction of an amide with a methanol to form an ester Draw all missing reactants and/or products in the appropriate boxes by placing atoms on the canvas and connecting them with b be created. L2 NH NHH
show the mechanism LIALH4 LEED 2 excess a Ho
7 Which molecule would react faster to answer. (HINT: you need to show the SLOW step of the mechanism.)(10 pts) CH3. H- 7 Which molecule would react faster to answer. (HINT: you need to show the SLOW step of the mechanism.)(10 pts) CH3. H-
please show me the mechanism for this question 1. LiAlH4 OME 2. acetone, HCI
Which alkyl halide would you expect to react more rapidly by an Sw2 mechanism? Show products and explain your answer. 1-bromooctane or 3-bromooctane
Select the species that you would expect to react and draw curved arrows to show the electron reorganization. Not all reactants shown are necessarily involved in the mechanism. Arrow.pushing Instructions ci:
draw reaction mechanism to form alcohol B by ketone reduction using diethyl ether solvent and LiAlH4 hydride reducing agent он OH Acid A Chemical Formula: CH 02 Molecular We ght: 135,15 Alcohol B Chemical Formula: CgH100 Molecular Weght: 122,16
please show all steps (a) Write the reaction mechanism for the hydrolysis of the amide under acidic conditions: 2 Et Н,о° heat OH + EtzNH2 Et (b) Write the reaction mechanism for the base catalyzed hydrolysis of the ester Na +n-BuOH OBu NaOH (aq)
What is the product of this reaction? Please show how you got this product. 1. LiAlH4, ether 2. H2O
Which alkyl halide would you expect to react more rapidly by and SN2 mechanism? Why? 1 which alkyl halide would you expect to eact nou rapidly by an Su2 mechanism? Why? a) n. Pribor vs. t-Bu Br b) i- Buch vs. n-Buch c) Lacive. ya