Acid-Catalyzed Hydration of 1-Hexene

Draw a structural formula of an alkene or alkenes (if more than one) that undergo acid-catalyzed hydration and without rearrangement give 1-methylcyclohexanol as the major product. • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • If more than one structure fits the description, draw them all. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate structures with + signs from the drop-down menu. ● VIL ? ChemDoodle Ⓡ Qt Sn [F

If ethanol was added to each of the following, which would be ineffective in preparing ethyl benzoate? Benzoyl chloride. Benzoic anhydride. Benzoic acid with catalytic sulfuric acid. Benzamide.     What is the stereochemistry of this compound?     2E, 5E 2Z, 5Z 2Z, 5E 2E, 5Z

15. Please help me answer this organic chemistry question

Briefly explain or give an introduction to this.   Structure Elucidation of Compounds using Several Spectroscopic Techniques. 1H and 13C NMR Spectroscopy IR Spectroscopy Mass Spectroscopy

Show a possible stepwise synthesis of 2, 3-dichloropentane starting with ethanol and propanol as the only sources of carbon atoms and any other inorganic reagents, solvents and laboratory equipment. Name the type of reaction that is occurring in each step of the synthesis.

6- In a 1H-NMR spectra on a scale of 0 – 10 ppm, Show the exact locations in ppm of 1-the saturated hydrocarbons, 2- the unsaturated hydrocarbons, 3- the halogenatedhydrocarbons and 4- the aromatic hydrocarbons.

Hydrohalic acids (i.e., HCl, HBr, HI) add to the double bond of alkenes to yield alkyl halides. Shown below is the carbon NMR spectrum of an alkene of formula C5H10. What is the structure of this alkene?

Draw a structural formula of an alkene or alkenes (if more than one) that undergo acid-catalyzed hydration and without rearrangement give 2-methyl-2-butanol as the MAJOR product. You do not have to consider stereochemistry. You do not have to explicitly draw H atoms. If more than one structure fits the description, draw them all. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate structures with + signs from the drop-down menu.

Draw a structural formula of an alkene or alkenes (if more than one) that undergo acid-catalyzed hydration and without rearrangement give 1-methylcyclohexanol as the major product. You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. ● If more than one structure fits the description, draw them all. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate structures with + signs from the drop-down menu. ● ● ✓ ? ChemDoodleⓇ n [ ]#

Predict the major organic product of 1,2‑dichloro‑3,5‑dinitrobenzene with sodium methoxide in methanol.

Draw a flowchart showcasing the purification step done for the reaction under basic conditions (the basic reaction of 4-methoxyacetophenone with bleach, sodium hydroxide, and acetone), starting from the crude reaction mixture all the way to the isolated solid product. Assume for this drawing that the reaction was complete, and that none of the intermediates are found in the crude mixture. There may still be however traces of your starting material in the crude mixture, along with any excess reagents

In the workup of the grignard reaction of turning bromobenzene to benzoic acid, we start by mixing the grignard with HCl and diethyl ether. We discard the aqueous layer and wash the organic layer with water. Then, the organic layer is extracted with NaOH. Then, the extracts are heated to remove ether. Then, it is precipitated with HCl. Precipitate collected. Let it dry and finally, purified with toluene and hexanes. Please make a flowchart of the process of this workup indicating what products and byproducts are forming. And what compounds are in the aqueous layer and organic layer in the steps.

12- Show (draw) or print or bring the 1H-NMR spectra and 13C-NMR and IR spectra formethyl ester.13- In a 1H-NMR spectra on a scale of 0 – 10 ppm, Show the exact locations in ppm of 1-the saturated hydrocarbons, 2- the unsaturated hydrocarbons, 3- the halogenatedhydrocarbons and 4- the aromatic hydrocarbons.

What factors during the experiment caused the percent yield to be different than 100%? What impurities may be present in the final product (look at the spectroscopic data for evidence of this), and how does that effect the percent yield calculation? I got 64% for the percent yield.

A student attempted to prepare 1-chlorobutane by mixing 1-butanol with NaCl in acetone. Was the student succesful? Explain.

Write a reaction that could be carried out to synthesize 1-(4-methylphenyl)ethanol (reactants will be a combination of Grignard reagent and carbonyl compound).

STARTING WITH 18MG OF 2-methyl-2-butanol JUST B PLEASE  (b) theoretical volume of alkene mixture (ml) expected to be obtained in this experiment.

Can you answer this question regarding this procedure: Discuss how bromobutane was made (the mechanism) and then how it was purified. Discuss success of the reaction in terms of yield and purity. Based on the mechanism, do you expect this to be a high yielding reaction? Why/why not? What could be changed (if anything) about the way the reaction was performed to increase the yield? Was the product isolated pure (discuss the IR)? Why was the product isolated the way that it was (what was the point of the different wash steps) and could it have been purified another way? Did the purification method cause significant loss of product (impacting the yield)? and if so, what could be done to prevent that in the future?

The ___________ functional group will have a sharp, dagger-like absorbance at 2220-2250 cm-1 on its IR spectrum (and an odd-numbered molecular mass (M+) on its mass spectrum).     alkyne     nitrile     aldehyde     alkene     carbolxylic acid

Some organic solvents do not work well in liquid-liquid aqueous extractions. Ethanol (HOCH2CH3) is a common inexpensive solvent, but is a poor solvent for extractions. In ten or fewer words, provide an explanation for why ethanol is a poor solvent selection for extraction. Hint: you may want to look up various properties of the molecule.

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1) Based on the Material Safety Data Sheets (MSDS) for the compounds, which of the compounds in this experiment is the most hazardous, and why (you have been given a representative aryl halide rather than all of the alkenes – as the products are all new, there’s not a simple answer to gauge their potential hazard)?  2,3-dihydrofuran,2-Mercaptobenzimidazole,Selectfluor, Dimethylformamide,dichloromethane-methylene chloride.