Samples used: n-butyl alcohol, sec-butyl alcohol, tert-butyl alcohol, acetaldehyde, n-butyraldehyde, benzaldehyde, acetone, acetophenone, isopropyl alcohol
Based on the samples used, which alcohol immediately forms 2 layers with the Lucas test? Why do you think this is so?
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Samples used: n-butyl alcohol, sec-butyl alcohol, tert-butyl alcohol, acetaldehyde, n-butyraldehyde, benzaldehyde, acetone, acetophenone, isopropyl alcohol Based...
Samples used: n-butyl alcohol, sec-butyl alcohol, tert-butyl alcohol, acetaldehyde, n-butyraldehyde, benzaldehyde, acetone, acetophenone, isopropyl alcohol Based on the samples used, which alcohol is most readily oxidized? Why d you think this is so?
Write a mechanism of the synthesis diisobutylene from tert-butyl alcohol with the use of elimination reaction. The following is the procedure of how it was done in the orgo lab: First of all, with the use of graduated cylinder 7mL of water was measured and then transferred in a 50mL round bottom flask. To the round bottom flask, it was added 7mL of sulfuric acid. The mixture was then cooled until the temperature got below 50 °C. In order to...
some we tested were propanal-methanal-acetone-cyclohexane-acetic acid-benzoic acid-methyl salicylate/n-butylamime--N,N-diethyaniline-nicotinamide-ethanamide/n-butylamine-N,N-diethylaniline-ethanol/2-propanal/tert-butyl-alcohol-phenol- Look at the solubilities of the compounds you tested. What could you say, in general. about the solubilities of these compounds based on the functional groups and number of carbons present? (Do not to simply list the solubility of every compound - the idea of this question is for you to offer a general conclusion)
I need help answering the following questions 1) A compound is insoluble in water, soluble in conc. H2SO4. It shows positive for the 2,4-DNPH test and negative for Chromic Acid test. What do you think the compound is? (3 pts) a) Isopropyl alcohol b) Butyraldehyde c) 3-pentanone d) butan-1-ol 2) Which compound would give a negative result for Iodoform Test? (3 pts) a) t-butyl alcohol b) Acetophenone c) 2-butanol d) Acetaldehyde 3) Which of the following routes can be used...
Explain why the IR corresponds to a particular compound of those that are possible based on BP and why it couldn't be any of the others -mention at least 3 IR peaks that are present that correspond to functional groups in your molecule, and discuss specific peaks that were either present or absent that allowed you to rule out the other compounds possible based on the boiling point. Reference your IR spectra as figures. the boiling point for unkown 2:...
In our experiment we will use three different substrates: 1°, n-butyl chloride; 2°, sec-butyl chloride; and 3°, tert- butyl chloride, and we will evaluate their reactivity and the rate of the reaction in an SN1 reaction. We will use an acid-base indicator to monitor the completion of the reaction and a salt, silver nitrate, to obtain a precipitate. The success of the reaction is evidenced by the change in color of the indicator (from orange to red) due to the...
GOING FURTHER 1. Based on the investigation, why do you think heat and alcohols are used to disinfecet medical equipment? 2. Sometimes when people accidentally ingest heavy metal ion like mercury they are asked to drink some milk. Why do you think this is? 3. How does a change in pH affect the secondary and tertiary structures of a protein? 4. Calculate the % Casein in your milk sample. (Show work) Suppose you filled one test tube with alanine and...
please help with how the flow chart will look like? thank you! Synthesis of n-Butyl Bromide Purpose of the Experiment: In this week's experiment you will be synthesizing n-butylbromide (IUPAC 1-bromobutane from 1-butanol and a concentrated acid via a nucleophilie substitution reaction. It is important to know that alcohols dehydrate to form alkenes in the presence of strong inorganic acids, so care must be taken in this experiment not to heat the reaction too vigorously else an elimination reaction may...
QUESTIONS 1. What is the purpose of the sulfuric acid (yes, it's a catalyst, but why is it a catalyst? What is it doing that makes the reaction possible? Would the reaction just go slower without it, or would the reaction not go at all? Why?) 2. If isobutyl alcohol (2 methyl propanol) is used instead of tert butyl alcohol, a mixture of products is obtained. One the products is the same as the product obtained with the tert butyl...
i believe its 3,3-dimethyt-2-butanol 0r 4 methylbeNzyl alcohol based on the data provided. if not which alcohol would it be for the unknown compunds. #3 Unknown Al Data unknown Melting point of solid ("C) (leave blank if liquid at RT): 57 degrees Celsius Boiling point of liquid (C) (leave blank if solid at RT) 0-H Stretch alcohol The results from sodium fusion and follow up ion tests (578) Predicted color Nitrogen test absent Nitrogen red brown precipitate Sulfur test black...