Question #b6602 Organic Chemistry Nucleophilic Substitution Reactions (SN1 and SN2) and Elimination Reactions (E1 and E2) E1 and E2 Reactions 1 Answer Ernest Z. Sep 20, 2016 Here's what I get. Explanation: a) #"CH"_3"CH"_2"CH"_2"-OH" + "SOCl"_2 → "CH"_3"CH"_2"CH"_2"-Cl" + "SO"_2 + "HCl"# b) #"CH"_3"CH"_2"CH"_2"-OH" + "POCl"_3 + "Py" → "CH"_3"CH=CH"_2 + "PyH"^+ stackrel(-)("O")"POCl"_2# c) #"CH"_3"CH"_2"CH"_2"CH"_2"-OH" + "HCl" stackrelcolor(blue)(Δcolor(white)(m))(→) "CH"_3"CH"_2"CH"_2"CH"_2"-Cl" + "H"_2"O"# Answer link Related questions What are E2 reactions? What are elimination reactions? Do E2 reactions change stereochemistry? How can I difference between substitution and elimination reactions? How do you distinguish between E1 and E2 reactions? What favors elimination reactions? Are elimination reactions favored at high temperatures? Are elimination reactions only organic reactions? Do the numbers 1 and 2 in E1 and E2 reactions relate to the number of steps in the elimination... What is reductive elimination in elimination reactions? See all questions in E1 and E2 Reactions Impact of this question 1700 views around the world You can reuse this answer Creative Commons License