Interpretation:
Propagation step should be written for the addition of hydrogen bromide to the 1-methy cyclohexene in the presence of a peroxide.
Concept introduction:
Radical or free radical: unpaired valence electron of an atom, molecule, or ion is called as radical.
Radical chain reaction takes place in three steps namely,
Initiation step –heat or light supplied, breaks the bond and creates radicals from a halogen molecule
Propagation step –radical from initiation step reacts with
Termination step –the combination of any two radicals resulting in all the electrons to be paired and thus the reaction gets terminated.
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Organic Chemistry
- Q1: Draw a valid Lewis structures for the following molecules. Include appropriate charges and lone pair electrons. If there is more than one Lewis structure available, draw the best structure. NH3 Sulfate Boron tetrahydride. C3H8 (linear isomer) OCN NO3 CH3CN SO2Cl2 CH3OH2*arrow_forwardIn the following molecule, indicate the hybridization and shape of the indicated atoms. -z: CH3 CH3 H3C HO: CI: :arrow_forwardQ3: Draw the Lewis structures for nitromethane (CH3NO2) and methyl nitrite (CH3ONO). Draw at least two resonance forms for each. Determine which form for each is the major resonance contributor. Page 1 of 4 Chem 0310 Organic Chemistry 1 Recitations Q4: Draw the Lewis structures for the cyanate ion (OCN) and the fulminate ion (CNO-). Draw all possible resonance structures for each. Determine which form for each is the major resonance contributor.arrow_forward
- Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage Learning