Give the products of reaction of cyclohexanone enolate with (a) iodoethane (reacts by C-alkylation) and (b) chlorotrimethylsilane, $\left(\mathrm{CH}_{3}\right)_{3} \mathrm{Si}-\mathrm{Cl}$ (reacts by $\mathrm{O}$ -silylation).
Added by Heidi R.
Step 1
Step 1: The reaction of cyclohexanone enolate with iodoethane (C-alkylation) will result in the formation of an alkylated product where the enolate carbon is attached to the ethyl group from iodoethane. Show more…
Show all steps
Your feedback will help us improve your experience
Grigoriy Sereda and 50 other Organic Chemistry educators are ready to help you.
Ask a new question
Labs
Want to see this concept in action?
Explore this concept interactively to see how it behaves as you change inputs.
Key Concepts
Recommended Videos
Give the expected products of the following acid-catalyzed reactions. (a) acetophenone $+$ methylamine (b) acetophenone $+$ dimethylamine (c) cyclohexanone $+$ aniline (d) cyclohexanone $+$ piperidine
Grigoriy S.
Predict the product, if any, of reaction between propanoyl chloride and the following reagents: (a) $\mathrm{Li}(\mathrm{Ph})_{2} \mathrm{Cu}$ in ether (b) $\mathrm{LiAlH}_{4}$, then $\mathrm{H}_{3} \mathrm{O}^{+}$ (c) $\mathrm{CH}_{3} \mathrm{MgBr}$, then $\mathrm{H}_{3} \mathrm{O}^{+}$ (d) $\mathrm{H}_{3} \mathrm{O}^{+}$ (e) Cyciohexanol (f) Aniline (g) $\mathrm{CH}_{3} \mathrm{CO}_{2}^{-+} \mathrm{Na}$
Draw the product formed when ethyl butanoate (CH$_3$CH$_2$CH$_2$COOCH$_2$CH$_3$) is treated with each reagent. With some reagents, no reaction occurs. a. SOCl$_2$ b. H$_3$O$^+$ c. H$_2$O, $^-$OH d. NH$_3$ e. CH$_3$CH$_2$NH$_2$
Recommended Textbooks
Organic Chemistry
Transcript
Watch the video solution with this free unlock.
EMAIL
PASSWORD