Aldehydes & Ketones Questions and Answers

Which reactions of Carbonyl compounds require a tight pH
Organic Chemistry
Aldehydes & Ketones Solutions
Which reactions of Carbonyl compounds require a tight pH control? Give the reaction, give the recommended pH range, explain why?
True False: The product of a hydrogenation reaction of an
Organic Chemistry
Aldehydes & Ketones Solutions
True False: The product of a hydrogenation reaction of an aldehyde or a ketone is an ester True False
Synthesize the following compounds from the given starting
Organic Chemistry
Aldehydes & Ketones Solutions
Synthesize the following compounds from the given starting material. You can add on on any alkyl/ alkyl halide under 8 carbons or any necessary inorganic reagent needed (this includes triphenyl
The correct statement regarding addition of sodium hydrogen
Organic Chemistry
Aldehydes & Ketones Solutions
The correct statement regarding addition of sodium hydrogen sulphite to a carbonyl compound is (A) The attack happens by the negative charge on oxygen (B) The rate of addition is always greater for
number of carbon atoms, while acetylene has an even number
Organic Chemistry
Aldehydes & Ketones Solutions
number of carbon atoms, while acetylene has an even number of carbon atoms A reaction shows acetylene with SMILES string C#C to form pentanal with SMILES string CCCCC=O. The transformation above can
From the table of reagents, select the reagents and
Organic Chemistry
Aldehydes & Ketones Solutions
From the table of reagents, select the reagents and conditions necessary to carry out the following reaction. 0²-0 a 9 OH Table of reagents a. NaBH, then H₂O* b. PBr3 c. Mg in dry ether, then CH₂-O,
Provide the structure of the product which results when the
Organic Chemistry
Aldehydes & Ketones Solutions
Provide the structure of the product which results when the alkene below is treated with O₂ followed by (CH3)2S. Draw the molecule on the canvas by choosing buttons from the Tools (for bonds), Atoms,
Draw a structural formula for the organic anion (i.e., do
Organic Chemistry
Aldehydes & Ketones Solutions
Draw a structural formula for the organic anion (i.e., do not include NH4) formed when ethanal is reacted with Tollens reagent. Don't forget the charge on the ion. . You do not have to consider
For each chemically-distinct set of protons in the following
Organic Chemistry
Aldehydes & Ketones Solutions
For each chemically-distinct set of protons in the following molecule, predict its a) relative integration, b) splitting pattern, and c) chemical shift (for example: 2H triplet @ 7.5 ppm).
1. a) Write a detailed mechanism for the formation of
Organic Chemistry
Aldehydes & Ketones Solutions
1. a) Write a detailed mechanism for the formation of dibenzalacetone. b) Give the IUPAC name of dibenzalacetone. c) Do you expect the configuration of the double bonds in this compound to be E, Z, or
Bismuth-214 can decay to form either polonium-214 or
Organic Chemistry
Aldehydes & Ketones Solutions
Bismuth-214 can decay to form either polonium-214 or thallium-210, depending on what type of radiation is emitted. Write a balanced nuclear equation for each process. Give all nuclei in the form X.
Draw the skeletal ("line") structure of
Organic Chemistry
Aldehydes & Ketones Solutions
Draw the skeletal ("line") structure of cis-5-methyl-2-hexene.