draw a mechanism and provide structure of the adol product that results when 4-methylpentanal is heated...
11) Provide the structure of the major organic product which results when PhCH2CHO is treated with NaOH 12) Provide the structure of the aldol product that results when 4-methylpentanal is treated with sodium hydroxide. 13) What two molecules were condensed in an aldol reaction to produce (CH3)3CCH-CHCOCH3? 1-4) Predict the outcome of the follovwing reaction. 0 0 NaOH, heat 15) Provide the structure of the ester that would undergo self-condensation to yield the B- ketoester shown below.
What product results when pentanal is heated with sodium hydroxide? Draw the molecule on the canvas by choosing buttons from the Tools (for bonds), Atoms, and Advanced by default. O * H: 120 EXP cont a H с N NN S ci
4.) Provide the structure of the major organic product that results when the reagents below are combined, and name the mechanism (SN1 or SN2) through which this reaction is proceeding (CH3)3N CH3CH2CH21 5.) Predict the product and show the entire electron pushing mechanism for the following reaction. In addition, name the mechanism (SN1 or SN2) through which it proceeds. ОН Hs HBr CH2CH2CH2CH2CH3 НзСH2C
The major product which results when 2-chloro-2-methylpentane is heated in ethanol is an ether. Provide the detailed, step-wise mechanism and name the product.
5. Draw the aldol condesation product when each of the following compounds are heated in the presence of aqueous sodium hydroxide solution. (a)
HW 22: Enolates 1. Provide a detailed, stepwise mechanism for the base-catalyzed enolization (keto enol tautomerism) of acetaldehyde. 2. Provide the major organic product of the folowing reaction. 3. Provide the major organic product of the following reaction LDA 4. Which of the following ketones will give a positive iodoform test? A) 4-heptanone D) cyclohexanone B) 3-hexanone C)2-hexanone 5. Provide the major organic product of the following reaction. 6. Provide the structure of the major organic product which results when...
Please help!!! 1) Provide the structure of the aldol product that results when 5-methylhexanal is treated with hydroxide.
Draw the structure of the product formed when the following compound is heated in aqueous base. The formula for the product is C8H12O.
The reactants are cyclopentanone and 4-methoxybenzaldehyde In the mechanism for the double adol condensation of (2E,5E)-2,5-bis(4-methoxybenzylidene)cyclopenanone using hydroxide as the base, does hydroxide act as a true catalyst? why?
Please draw out structure and label spectra NaoH HA H2O CH3 Ketone Aldehyde Adol condensation product Product 'H NMR: area=3 areal areas area = 2 area = 2 area=1 2 area PPM