Dehydration of Alcohols Dehydration of 2-Methylcyclohexanol Prelaboratory Mole Calculations Calculate the theoretical yield of the cyclohexenes...
calculate the theoretical yield of the cyclohexenes products
in both miles and grams
Dehydration of Alcohols Dehydration of 2-Methylcyclohexanol Prelaboratory Mole Calculations Calculate the theoretical yield of the cyclohexer of the starting alcohol gives one mole the mixture of isomers. toles and grams. One mole sing 1.0 mL of 2-methylcyclohexanol and 0.5 mL of the catalyst, H3PO4. NO calculation is needed for the catalyst. OH Н,РО, Third product CH12 one double bond + H2O heat 2-methylcyclohexanol bp 165-168°C d=0.93 g/mL...
Experiments Dehydration of 2-methylcyclohexanol Questions 1. Please answer this question on notebook paper, not in the lab sometimes dimicult to read.) tebook (carbon copies are Consider the phosphoric acid-catalyzed dehydration of the following list of nine alcohols. Give the structure of each alcohol and that of the resultant alese. If a MIXTURE of alenes is anticipated. give both products and circle the major product (a) Cyclohexanol: (b) 1-methylcyclohexanol (c)2-methylcobecnold 3-methylcyclohexanol: (e) 4-methylcyclohexanol: (cyclopentanol (R) 3- canotth) 2-pentano: 0) 3-pentanol. 2....
I
am writing a prelab for this experiment, but am struggling on how
to figure out what the balanced
chemical equation is. Any help is much appreciated, thank you!
DEHYDRATION OF 2-METHYLCYCLOHEXANOL Prelab: Do parts 1-3 including finding the limiting reactant and theoretical yield. You will not get credit for your prelab if you do not do this. You must also write out the balanced equation. The one given below is not balanced. Read: Organic Chemistry by Carey, p. 250-257;...
please help
The dehydration of alcohols Under acidic conditions, alcohols will undergo a dehydration reaction, producing an alkene and water. During the reaction, the hydroxyl group of the alcohol and a hydrogen atom from an adjacent carbon atom are lost. The reaction takes place in three steps, as shown in the diagram. (Figure 1) In the first step, a hydrogen lon bonds to the hydroxyl group of the alcohol. In the second step, the protonated hydroxl group leaves the compound,...
how does the mixture of isomeric alkenes produced by an
acid-catalyzed dehydration reaction compare with the alkene mixture
from a base-catalyzed dehydrochlorination reaction? Are either or
both sets or products influenced primarily by product
stability?
E1/E2 Elimination Reactions. Acid-Catalyzed Dehydration of 2-Me Base-Catalyzed Dehydrochlorination of 2-Chloro-2-methylbutane Acid-Catalyzed Dehydration of 2-Methyl-2-butanol and Adapted for an experiment published in More J.R - Hammond, C.N. Schatz, PF: Morrill, T.C.: Modern Projects and P. Hammond CN: Schatz, P.F., Morrill... Experiments in Organic Chemistry, 2nd...
can you help me calculate the theoretical yield calculations for
2 methoxyphenol and 3-chloro-1,2-propanediol
THE laboratory The essential reactants guaifenesin synthesis are provided in Table 1. Table 1. Compound 2-methoxyphenol bp (°C) Reactants used amount used mmol 550 L calculate MW 124.14 d (g/mL) 1.13 NaOH (25% soln.) 40 do 1 mL obno ethanol 46.07 18 water 142.04 1.32 Sodium sulfate calculate 110.54 500 L (+)-3-chloro-1,2- propanediol 164
Need help with number 2 and 3 on the postlab section.
Elimination Reactions Background The purpose of this lab is to prepare an alkene by dehydration of an alcohol in the presence of an acid catalyst Elimination reactions often result in the formation of multiple products. In this lab, 2-methylcyclohexanol is dehydrated to form an alkene. The product will be analyzed by GC-MS to determine the ratio of alkene isomers formed. You will need to determine the mechanism of the...
HO CH сн. CH2 нс HC CH3 HAC-HC CH CH CH CH d) OH OH 13. The labels have fallen off three bottles. Bottle A contains a gas, bottle B contains a liquid, and bottle C contains a solid. The labels indicate that the compounds have the same number of carbon atoms, one being an alkane, one an alcohol, and the other a carboxylic acid. Suggest the identity of the contents of each bottle, and give reasons for your explanation...
What is the theoretical yield (in grams) and percent yield of your
triphenylmethanol product in this experiment? (Weight of
triphenylmethanol: 0.060g)
BACKGROUND AND THEORY The Grignard reaction was one of the first organometallic reactions discovered and is still one of the most useful synthetically. By reacting an organohalide (usually a bromide) with magnesium in ethereal solvent, carbon becomes a nucleophile. Grignard reagents are the starting points for the syntheses of many alkanes, primary, secondary, and tertiary alcohols, alkenes, and carboxylic...
What is answer of #10??
Report: Hydroboration of 1-Methylcyclohexene Mechanism / GC Analysis / Calculations 1. After reviewing the GC and 'H NMR spectra, what is the major product of the reaction? + 3 a. BH: . THF 3 b. 3 H2O2 OH + 3 OH c. NaOH MOH OH racemic racemic major 2. Draw the complete curved arrow mechanism for the reaction to produce the major product, including both the hydroboration and oxidation steps. Repetitive steps need only be...