Match the following reagents with the use they have in their respective reactions. A good molecule for aldol condensation. Choose... The Grignard reagent Choose... HCI A good functional group for reductive amination Magnesium metal Benzaldehyde A very strong reductant para-toluidine A catalyst for Fischer esterification NABH4 RM9X A good reagent for an EAS. N,N-dimethyl aniline Sulfuric acid aldehyde

Match the following reagents with the use they have in their respective reactions. A good molecule for aldol condensation. Choose... The Grignard reagent Choose... HCI A good functional group for reductive amination Magnesium metal Benzaldehyde A very strong reductant para-toluidine A catalyst for Fischer esterification NABH4 RM9X A good reagent for an EAS. N,N-dimethyl aniline Sulfuric acid aldehyde

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

See similar textbooks

Similar questions

Draw the major product of the aldol addition reaction between two of equivalents of this aldehyde with the conditions provided. Ignore inorganic byproducts. 1. NaOH H 2. Neutralizing work-up Atoms, Bonds and Rings Charges Draw or tap a new bond to see suggestions. Undo .༡ Reset > Remove Done Drag To Par
The compound below exists in two tautomeric forms. Circle the most acidic proton in the keto formbelow and draw the enol tautomer of the compound.
Does the reaction between phenol and dess martin periodine will happen? If not why?
under each compound write "activating" or "deactivating" rings. "ortho-para" por ortho-para directing rings, or "meta" for meta-directing rings. Also write "No F.C." under any compound that will not undergo friedel-craft acylation or alkylation
C. Using any necessary reagents of 2 carbons or less, and any other necessary inorganic reagents, synthesize this compound.
Which of the following is a limitation of the Friedel-Crafts reaction? Select one: O A. The carbocation electrophile can potentially undergo an unwanted rearrangement prior to its bonding to the aromatic ring. OB. Poly-alkylation products form when aromatic reactant and alkylating agent are mixed together in comparable amounts. OC. A Friedel-Crafts reaction fails when the aromatic starting compound contains a moderately or strongly deactivating group. OD. All of the above choices are limitations of the Friedel-Crafts reaction.
need explanation
Which of the following aldehydes does not undergo an aldol condensation when mixed with base? A. (CH3)3CCHO B. C6H5CH2CHO C. CH3CHO D. CH3CH2CHO
I specifically need help on sub-parts d, e, f, g, and h.
Which of the given enolates can not be formed during the course of following aldol reaction? flor CH3 a. b. О с. Lov CH3 H₂C² FCH₂ + CH₂CH3 H3C CH₂CH3 NaOH
Propose how you might synthesize the following molecules from an alkyl halide and a nucleophile.
What conjugate base must be formed during the E1cb mechansim in an aldol condensation reaction running under basic conditions? А. enol В. B-hydroxy carbonyl C. a,B-unsaturated carbonyl D. enolate