Interpretation:The mistake made in procedure that might result in appearance of unusual red-orange solid should be identified.
Concept introduction:Alkenes are considered electron-rich and undergo bromination addition reaction with
The mechanism of
In the second step, the strained bromonium ion intermediate opens while
The bromination of
yields four stereoisomers illustrated as follows:
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EBK EXPERIMENTAL ORGANIC CHEMISTRY: A M
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- 20:24 1 : 10. Draw the full cleavage of 2-ethoxypropane by HCI scheme on your paper, and then draw in the curved arrows for each step of the mechanism. HICI co OⓇ ← H₂O 11. What reagent can be used to convert 2-methylbutan-1-ol into 2-methylbutanal? A) Bleach B) LIAIH4 C) DMSO, (COCI)2, TEA D) Na₂Cr₂O7, H₂SO4 E) 03 12. Fill in the box with the major organic product of the first step of the reaction shown? H-Cl Send a chat Oarrow_forwardQUESTION 18 Consider the ether cleavage reaction shown below. What mechanism occurs and what are the major organic products of the reaction? 1 eq. HCI ponding letter designation O A. Mechanism: S2, Products: B.. Mechanism: SN1, Products: OC. Mechanism: SN1, Products: CI HO D.. Mechanism: SN2, Products: HOarrow_forwardDraw all the resonance forms for the sigma complexes corresponding to bromination ofaniline at the meta, and para positionsarrow_forward
- V. What is the mechanism of this?arrow_forwardd) Explain why product C is racemic but product D is non-racemic. Br CH,OH fonnet Siz mechinmwhin mes in inversion of the procdnct odue to Hhen bukside ata from the Mactoprile Br NaSH Darrow_forwardPlease deaw structures of the resonance structures of "enolate" of the following compounds with "a-H's" . Each has more than one kind, so choose the a-H marked (*). Thank you!arrow_forward
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