Be sure to answer all parts. Synthesize the product starting from benzene. [C] [A] [D] [F] [G] A CH,CH,C1 AIC13 [D] draw structure ... KOC(CH3)3 draw structure ... [A] draw structure ... [B] [E] Cl₂ FeCl3 [G] [E] [B]+ [o isomer] mCPBA draw structure ... draw structure ... draw structure ... [C] [F] H₂SO4 [C] NO₂ draw structure ...

(10, 6) Draw structural formulas for all of the enol forms of the carbonyl compounds below. You do not have to consider stereochemistry. Consider stereoisomeric enols as a single enol form. In the case of dicarbonyl compounds, do not include stuctures in which both carbonyl groups are present as enols.

Examine the reactant and product for each reaction. Label each transformation as an addition, elimination, or substitution. Br А. Br ОН elimination addition С. substitution D. B.

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Considering that sulfur is just below oxygen in the periodic table, which compound will react the third fastest with fuming sulfuric acid? H°OS O b. d.

What is the name of these compounds?

Arrange these compounds in order of increasing boiling point. Values in °C are 36, 78, 129, and 214. 36°C 78°C 129°C 214°C Drag and drop your selection from the following list to complete the answer: CH3 CH₂OH C5 H12 CH3 CH₂ CH(CH3)CH₂OH HOCH₂ CH₂ CH₂OH

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( do 4 5 6 7 with exaplanation plz

Using the periodic table of elements answer the following: A) either 2-methyl propane is converted to 2-bromo-2methyl propane by reaction Br2 in presence of UV light B) or 2-methyl propensity is converted to 1-chloro-2methyl-2-propanol by reaction with an aqueous solution of chlorine (Cl2)