Can someone please explain the answer clearly? 16) Which hydrogen atom in the molecule shown below will be most readily abstracted by abromine radical to produce a carbon radical?HaHpНаHcНа

We have to find the H atom that will be most readily abstracted by a bromine radical to produce a…

Answered: Which hydrogen atom in the molecule…

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter15: Radical Reactions

Section: Chapter Questions

Problem 6E

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Compounds containing a phenol group may work as ANTIOXIDANTS to prevent free radical damage. This is accomplished when a free radical (or UV light) encounters a phenol group, turning the phenol group into a radical. However, contrary to typical radical behavior, the structure of the phenol radical can neutralize (or quench) the unpaired electron. Specifically, the phenol structure neutralizes (or quenches) the unpaired radical electron by doing the following: taking the electron and The correct name (or abbreviation) of an example compound (discussed in the lecture videos) containing a phenol group with antioxidant properties is:
Which of the following processes could be the termination step in free radical substitution reaction? C2H6 --> 2CH3∙∙ ∙∙CH3 + ∙∙CH3 →→ C2H6 C2H6 + H∙∙ →→ H2 + C2H5∙∙ ∙∙C2H5 →→ C2H4 + H∙
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Please answer this organic chemistry question: show all three steps and radical mechanism for hydrobromic acid in peroxide reacting with 3-methylene-2-ene. Are there multiple products? Background information just in case needed for the intial question above ? but if not needed just ignore this background information: which of the following compounds will react the quickest? A) Fluorine with a tertiary radical B) chlorine with a tertiary radical C) Bromine with tertiary radical D) chlorine with a primary radical E) bromine with a primary radical
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omplete the following mechanistic steps (#1 through 4) representing every step of the echanism: The radical chain begins (initiation) with the photochemical cleavage of a Br-Br bond, affording two bromine atoms (Br ): Br-Br Br Then, the propagation steps take place. First, the bromine atom reacts with the substrate to afford a resonance-stabilized benzylic radical. Represent this process and the different resonance forms of the resulting radical: СООН + Br HBr +
Allylic bromination of alkenes is accomplished with the reagent NBS (N-bromosuccinimide). The reaction proceeds by a radical chain mechanism. For the following reaction: NBS Br light, CCI4 a Select the species that you would expect to react in the first propagation step and draw curly arrows to show the mechanism. Use half-headed (fishhook) curved arrows to show electron reorganization. When drawing bond formation by pairing of single electrons, terminate the arrows in a hotspot located to one side of a reacting radical. This hotspot is not associated with any structural feature. Arrow-pushing Instructions 将一郎: Br H2 Previous Next
Please help me with this organic chemistry question: which of the following compounds will react the quickest? A) Fluorine with a tertiary radical B) chlorine with a tertiary radical C) Bromine with a tertiary radical D) chlorine with primary radical E) Bromine with primary radical
In theory, there are only three inequivalent hydrogens in this molecule that could be substituted by Br in a free radical bromination – circle them. Put an asterisk to mark the one most likely to be substituted first.
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Chemistry Glutathione (or GSH) can form a disulfide bridge with another glutathione molecule via radical reaction. Show a mechanism of a hydroxide radical reacting with two glutathione molecules to a produce a dimer (GSSG).

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Which hydrogen atom in the molecule shown below will be most readily abstracted by a bromine radical to produce a carbon radical? Ha Ho На Ho На