Help please 7- What do you use to create a tertiary alcohol using the Grignard reaction?a- A ketoneb- An aldehydeC- An alcohola- A carboxylic acid8- Which of the following compounds shown below do you expect to dissolve in10% HCI? (NH2OH123OH

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Answered: 7- What do you use to create a tertiary…

Organic Chemistry

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ISBN:9781305080485

Author:John E. McMurry

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Chapter4: Organic Compounds: Cycloalkanes And Their Stereochemistry

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Problem 62AP: Alcohols undergo an oxidation reaction to yield carbonyl compounds on treatment with CrO3. For...

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Draw structural formulas for the major organic product reaction
Use the following reagent table for the reaction of : cyclohexanol + H2 SO4 → cyclohexene Chemical MW (g/mol) Density (g/mL) mmols used Amount used cyclohexanol 100.16 0.9624 1.50 mL Sulfuric Acid 98.08 1.83 1.0 mL cyclohexene 82.14 How many mmols of sulfuric acid are used? (answer with 2 decimal places, no units)
Please complete the last row
HgSO4 H2SO4, H20 1T (1) Br H2O2, NaOH 10 NaNH2 BH3, THE H =H 1S NH3 H20 HCI (1 equiv.) diethyl ether 1V 1W Br2 (m) MgBr (H,C=CH),CULI NaOCI ТСРВА > 1X 1Y > 1Z CH3COOH 1AA diethyl ether SoCI2, pyridine diethyl ether 1AB
116. Subject :- Chemistry
Ff.179.
Alcohols undergo an oxidation reaction to yield carbonyl compounds on treatment with CrO3. For example, 2-tert-butylcyclohexanol gives 2-tert-butylcyclohexanone. If axial OH groups are generally more reactive than their equatorial isomers, which do you think reacts faster, the cis isomer of 2-tert-butylcyclohexanol or the trans isomer? Explain.
Complete the following acid-base reactions. (a) CH3CH2CH2CH2Li + CH3COOH (b) CH3CH2CH2CH2MgBr + CH3CH2OH
17-73 Alcohols can be prepared by the acid-catalyzed hydration of alkenes (Section 12-6B) and by the reduction of aldehydes and ketones (Section 17-4B). Show how you might prepare each of the following alcohols by (1) acid-catalyzed hydration of an alkene and (2) reduction of an aldehyde or a ketone. (a) Ethanol (b) Cyclohexanol (c) 2-Propanol (d) 1-Phenylethanol
14-71 The mechanism of the acid-catalyzed dehydration of an alcohol to an alkene is the reverse of the acid- catalyzed hydration of an alkene. The dehydration mechanism occurs by the following three steps. Step 1: Add a proton. Step 2: Break a bond to form stable molecules or ions. Step 3: Take away a proton. These three steps are illustrated here by the dehydration of 2-butanol to give 2-butene. Use curved arrows to show the flow of electrons in each step; that is, show how each bond-making or bond-breaking step occurs. H I + Step 3: CH3—CH—CH—CH3 CH3—CH=CH—CH3 + H + 2-butene
Another important pattern in organic synthesis is the construction of CC bonds. Using your reaction roadmap as a guide, show how to convert propane into hex-1-en-4-yne. You must use propane as the source of all of the carbon atoms in the hex-1-en-4-yne product. Show all reagents needed and all molecules synthesized along the way.
The amount of tartaric acid is responsible for the tartness of wine and controls the acidity of the wine. Tartaric acid also plays a very significant role in the overall taste, feel and color of a wine. Tartaric acid is a diprotic organic acid The chemical formula for tartaric acid is C4H6O6 and its structural formula is HO2CCH(OH)CH(OH)CO2H. A 50.00 mL sample of a white dinner wine required 21.48 mL of 0.03776 M NaOH to achieve a faint pink color. Express the acidity of the wine in terms of grams of tartaric acid, H2C4H4O6 (M. M. = 150.10) per 100 mL of wine. Assume that the two acidic hydrogens are titrated at the end point. MM H2C4H4O6 = 150.10 MM NaOH = 40.00 Below is the balanced chemical equation for this titration.

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7- What do you use to create a tertiary alcohol using the Grignard reaction? a- A ketone b- An aldehyde C- An alcohol a- A carboxylic acid 8- Which of the following compounds shown below do you expect to dissolve in 10% HCI? ( NH2 OH 1 2 3 OH