Problem A 3. Predict the products of each reaction.A) toluene + 1) NBS, ROOR, A; 2) Mg/ether; 3) CH3CH₂CHO (aldehyde); 4) H³O*, A →B) 2-phenylpropane + 1) KMnO4, OH, A; 2) H3O* -C) chlorobenzene + 1) H₂SO4 (conc); 2) HNO3; 3) H₂O*, A→

Here we have to predict the final major product formed in the following given sequence of reactions.

3. Predict the products of each reaction. A) toluene +1) NBS, ROOR, A; 2) Mg/ether; 3) CH3CH₂CHO (aldehyde); 4) H3O*, A → B) 2-phenylpropane + 1) KMnO4, OH, A; 2) H3O* → C) chlorobenzene + 1) H₂SO4 (conc); 2) HNO3; 3) H₂O*, A→

3. Predict the products of each reaction. A) toluene +1) NBS, ROOR, A; 2) Mg/ether; 3) CH3CH₂CHO (aldehyde); 4) H3O, A → B) 2-phenylpropane + 1) KMnO4, OH, A; 2) H3O → C) chlorobenzene + 1) H₂SO4 (conc); 2) HNO3; 3) H₂O*, A→

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter6: Alkanes & Alkenes

Section: Chapter Questions

Problem 33CTQ

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Organic synthesis is a branch of chemical synthesis that involves the planned construction of organic compounds/molecules from smaller units that possess functional groups. Friedrich Wöhler was the first scientist who designed the synthesis of an organic compound, urea from inorganic starting materials silver cyanate with ammonium chloride via a simple, one-step synthesis.

Question

Problem A

3. Predict the products of each reaction.
A) toluene + 1) NBS, ROOR, A; 2) Mg/ether; 3) CH3CH₂CHO (aldehyde); 4) H³O*, A →
B) 2-phenylpropane + 1) KMnO4, OH, A; 2) H3O* -
C) chlorobenzene + 1) H₂SO4 (conc); 2) HNO3; 3) H₂O*, A→

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