When a mixture of aldehyde RCHO and an excess of alcohol R'OH is treated with an acid catalyst, which of the following is the product formed? O a. R'O OH Ob. R'O O C R OC. R'O OR R Od. R'O R 'Н OH OR 'H QUESTION 11 When a mixture of aldehyde RCHO and an excess of alcohol R'OH is treated with a base catalyst, which of the following is the main product formed? OB. R'O OH Ob. R'O OR R OH OC. RO OR H Od. R'O O R H Click Save and Submit to save and submit. Click Save All Answers to save all answers. 18 stv P

When a mixture of aldehyde RCHO and an excess of alcohol R'OH is treated with an acid catalyst, which of the following is the product formed? O a. R'O OH Ob. R'O O C R OC. R'O OR R Od. R'O R 'Н OH OR 'H QUESTION 11 When a mixture of aldehyde RCHO and an excess of alcohol R'OH is treated with a base catalyst, which of the following is the main product formed? OB. R'O OH Ob. R'O OR R OH OC. RO OR H Od. R'O O R H Click Save and Submit to save and submit. Click Save All Answers to save all answers. 18 stv P

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter19: Eas: Electrophilic Aromatic Substitution

Section: Chapter Questions

Problem 7E: When toluene is treated with sulfuric and nitric acids under special conditions, three nitro (NO2)...

See similar textbooks

Similar questions

When toluene is treated with sulfuric and nitric acids under special conditions, three nitro (NO2) groups are substituted for hydrogens at the 2, 4 and 6 positions on the ring (the next section discusses why the 2, 4, and 6 positions are substituted). The product is a highly explosive substance called 2,4,6-trinitrotoluene. This subastance is commonly known by a three letter name. What is it?
What is the correct reaction scheme look like between acetic acid and 3-methylbutanol in the presence of sulfuric acid? Which image attached is the correct reaction scheme?
Can you help me number 8 part A ? Which is the formula of this rule of reaction (decarboxylation reaction)?
Write the structural formula of the organic product for the given reaction between an alkyne and an alkyl halide. The alkyne group is shown and should be entered as "CC" without the triple bond. Enter CC before associated HH atoms (e.g., CH3CH2CH2OCHCHCH3). what is the name of the product. 1.NaNH2 CH3CH2CCH------> product 2. CH3CH2Br
This image is the final product that is produced. If a synthesis started with benzene and other organic compounds (four carbons or less) what would the synthesis look like to achieve this final product.
For Fehling's Test not all aldehydes reacts to this test, what are the limitations and does the samples given below reacts to Fehling's Test? Explain a. formaldehyde b. glucose c. benzaldehyde d. acetone
1-butanol is reacted with PCC and carried out with an anhydrous solvent DCM, what is the intermediate and product of this reaction
What type of synthesis is this an example of? Is this showing the addition of a ketone giving a tertiary alcohol? If so, how come an ether is not needed for this synthesis?
Fill in the blanks with the MAJOR organic product in the following reactions.
Alcohols react with sulfonyl chlorides to form sulfonate esters. Only the O-H bond of the alcohol is broken in the reaction, and so no inversion of configuration occurs. The resulting sulfonate esters are reactive in SN1 and SN2 reactions since the sulfonate group is a very weak base and is therefore a good leaving group.Draw curved arrows to show the movement of electrons in this step of the mechanism.
Please solve correctly: Optio for Q1. a.)2-hexyne b.)3-methyl-1-pentyne c.)3-hexyne d.)1-hexyne e.)4-methy-1-pentyne Q2) a.)Alkenes react with nucleophiles and bases. b.)Alkenes react with electrophiles. c.)In the reactions of alkenes, the p bond is not always broken. d.)Alkenes contain double bonds from two sp-hybridized carbon atoms.
QUESTION 8 What reagent and condition are required to convert dicyclobutyl ketone to di-cyclobutyl methanol? A. KMnO4, acetone, H3O+ B. Propanoic acid, HCl, 30oC ? C. NaBH4, ethanol, H3O+ D. CH3CH2MgBr, ether, H3O+