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Which of the following molecules might be prepared as final product, by using an aldol condensation...
Which of the following molecules might be prepared as final product, by using an aldol condensation reaction to condense an aldehyde with itself? CH 0 H CHO CH 0 HC CH Н HC CHE CH HC CHE NI a E (hp 00
In the dehydration experiment, which statement is true? Phosphoric acid may be the limiting reagent. The rate determining step involves the protonation of the alcohol. Drierite use helps improve the yield Heating the reaction mixture above 160 C will not change the product distribution Question 4 (3 points) Which of the following molecules might be prepared as final product, by using an aldol condensation reaction to condense an aldehyde with itself? CH, 0 H₂C. H H₂C H CH3 H₃C. CH3...
Be sure to answer all parts.
Can the aldol addition product of the aldehyde below undergo an
aldol condensation reaction? Why or why not?
If a reaction occurs, draw the structure of the aldol
condensation product. If not, write NR.
Be sure to answer all parts. Can the aldol addition product of the aldehyde below undergo an aldol condensation reaction? Why or why not? If a reaction occurs, draw the structure of the aldol condensation product. If not, write NR....
1. Each of the following compounds can be prepared by a mixed aldol condensation reaction. Give the structures of the aldehyde and/or ketone precursors for each aldol product, identifying the electrophilic partner and nucleophilic partner. (6 Points) Electrophilic partner Nucleophilic partner Electrophilic partner Nucleophilic partner Electrophilic partner Nucleophilic partner
1) Which of the following molecules would not undergo an aldol condensation with itself? Circle each that apply (3 points) CH, OCH, H 2) How could the following crossed-aldol condensation be performed to obtain the product selectively? Devise a method, and detail what to do in the lab below. Also include a full mechanism. (5 points) S. 7-8 4) Provide a complete, electron-pushing mechanism for the reactions shown below (7 points each) (1) "omo (2) H30 HOCI
Match the starting ketone or aldehyde with appropriate product
of either aldol addition or adol condensation reaction.
A ketone or an aldehyde from the list undergo either aldol addition (in a case aldol addition product can not undergo further elimination) or aldol condensation reaction in protic solvent under basic catalysis. Match the starting ketone or aldehyde with appropriate product of either aldol addition or aldol condensation reaction propanal acetaldehyde 2-ethyl-2-hydroxy-hexanal 2-methylbuta ethanal Please answer 2-ethyl-4-methyl 2-hexenal Choose 2-methyl-2-pentenal 2-ethyl-3-hydroxy-2,4-dimethyl hexanal...
which of the following molecules cannot undergo an
intramolecular aldol condensation when treated with NaOH
Which of the following molecules cannot undergo an intramolecular aldol condensation when treated with NaOH
#4 which of the following represent the final product of the
below aldol condensation reaction ? the IR of the product does not
have a broad peak around 3300 wavenumbers
Which intermediates are formed during the mechanism of the below reaction? Select all that apply. 2 й — ДА . с . CH_CH3 \ 2. То No ті о он g / H,с сну Нас сн, о - — -- H₃C CH₂ Question 2 2 pts In the above reaction,...
What is the aldol condensation product of cyclohexanone as the ketone and benzaldehyde as the aldehyde? Show the MECHANISM, REACTION, and provide NAME of product.
QUESTION 1 Which of the following will not undergo an aldol condensation reaction? butanal C 2-methylbutanal C 2,2-dimethylbutanal 3,3-dimethyl-2-butanone QUESTION 2 Which of the following constitutes a difference between an aldol and a Claisen condensation? basic conditions Ctetrahedral intermediate Cenolate ion formation protonation of the intermediate QUESTION 3 The product of an aldol condensation reaction is generally favored if Can unsymmetrical ketone and aldehyde are used Can unsymmetrical ester and ketone are used Cone of the carbonyl partners contains no...