what is the mechanism for 2-ethyl-3-hydroxy-hexanol? please show electron arrows. The starting materials are acetaldehyde, butanol, EtOH, KOH Thank you
what is the mechanism for 2-ethyl-3-hydroxy-hexanol? please show electron arrows. The starting materials are acetaldehyde, butanol,...
Calculate the following chemicals boiling point at 5000 kPa N-Butanol, 2-ethyl Butanol, 2-ethyl Hexanol, Hexanol, Octanol [please add the reference if you can]
1. Propose a mechanism: Starting material: butyraldehyde Solvent: water Reagent: Potassium Hydroxide(KOH) Final product: 2-ethyl-3-hydroxy-hexanal 2. Propose a mechanism: Starting material: Methyl Propionate Solvent: water Reagent: HCl Final product: propionic acid
please show the reaction completely with arrows please b) The reaction of ethyl acetate with butanol to produce butyl acetate using hydronium and water 17
Starting with the alkane (butane), please work the mechanism to get the final, aldehyde product. Please DRAW OUT the detailed mechanism and show ALL ELECTRONS on the reagents and the reactants along with the arrows pointing to the exact atom the electron(s) are being transferred to. Thank you SO MUCH in advance. I just really want to understand the mechanisms how the reagents rearrange the molecules via electron pushing. 0 OH butyraldehyde 1-butanol DMP NaOH Br Br 1-bromobut-2-ene 1-bromobutane H2/Pd,...
What is the IUPAC name of the given molecule? OH Br 1-bromo-2-ethyl-2-hydroxy-3-methylpentanoic acid 2-ethyl-3-methylpentan-2-ol-1-carboxyl bromide 2-ethyl-3-methyl-2-ol-pentanoyl bromide O2-ethyl-2-hydroxy-3-methylpentanoyl bromide What statement is TRUE about the mechanism for the reaction shown here? CH,(CH)2CO,CH, NaOH CH3(CH12COCH excess heat CH3(CH)2CO,CH2 Water attacks the carbonyl carbon to form a tetrahedral intermediate. The first step of the reaction involves protonation of the ester carbonyl oxygen. One of the products formed is glycerol. The hydroxide deprotonates the alpha carbon. Which bases among the following is/are used...
Using retro synthesis what alkyl halide and ketone were used to produce 3-ethyl-3-hexanol. The two starting materials cannot be 1-bromopropane and 3-pentanone. Calculate the percent yield of the final product which weighed 0.16g. The starting weight of Magnesium was 0.612g and starting weight of Ammonium Chloride was 0.6012g.
Draw curved arrows to illustrate the mechanism for the following reaction of 3-ethyl-3-pentanol and HCI. The starting material and intermediates have been pre-drawn for your convenience. tcl
3. Write a detailed mechanism to yield 3-methyl-2-oxacyclopentanone. What is the hydroxy acid (starting material) for this lactone formation? Hydroxy acid
please show the mechanisms involved (using arrows to show all electron movements) and give the product(s) for the reaction below. also name the starting material, if possible. H2NNH2 KOH H2NNH2 KOH
Using curved arrows, show the mechanism of preparing 2-ethyl-3- methylbutanoic acid via the Malonic Ester Synthesis route.