Interpretation:
For the given transformation a reasonable mechanism need to be drawn.
Concept introduction:
Aldol condensation reaction is where the aldol addition product undergoes dehydration to give a conjugated enone. In
- Deprotonation of carbon
- Attach of enolate ion with the
aldehyde (nucleophilic attack) - Protonation of the alkoxide ion to give aldol product
- Dehydration of the aldol addition product to form conjugated enone (aldol condensation product)
If the aldol condensation reaction takes place between two carbonyl compounds it is known as intermolecular aldol condensation reaction and if the same takes place within a single molecule means it is known as intramolecular aldol condensation reaction.
Retrol-Aldol process is the one in which the intermediates formed are the same but they appear in reverse order compared to Aldol condensation process.
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Chapter 21 Solutions
ORGANIC CHEMISTRY-NEXTGEN+BOX (2 SEM.)
- Draw the curved-arrow mechanism with the drawings of the molecules, not just abbreviations. -NO₂ Sn, HCl (aq) E D H (CH3CO)₂O -NH2 CH3arrow_forwardWhat is/are the product(s) of the following reaction? Select all that apply. * HI A B C OD OH A B OH D Carrow_forwardIn the image, the light blue sphere represents a mole of hydrogen atoms, the purple or teal spheres represent a mole of a conjugate base. A light blue sphere by itself is H+. Assuming there is 2.00 L of solution, answer the following: The Ka of the left & right solution is? The pH of the left & right solution is? The acid on the left & right is what kind of acid?arrow_forward
- What spectral features allow you to differentiate the product from the starting material? Use four separate paragraphs for each set of comparisons. You should have one paragraph each devoted to MS, HNMR, CNMR and IR. 2) For MS, the differing masses of molecular ions are a popular starting point. Including a unique fragmentation is important, too. 3) For HNMR, CNMR and IR state the peaks that are different and what makes them different (usually the presence or absence of certain groups). See if you can find two differences (in each set of IR, HNMR and CNMR spectra) due to the presence or absence of a functional group. Include peak locations. Alternatively, you can state a shift of a peak due to a change near a given functional group. Including peak locations for shifted peaks, as well as what these peaks are due to. Ideally, your focus should be on not just identifying the differences but explaining them in terms of functional group changes.arrow_forwardQuestion 6 What is the major product of the following Diels-Alder reaction? ? Aldy by day of A. H о B. C. D. E. OB OD Oc OE OAarrow_forwardNonearrow_forward
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