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S  0 ``  >*  0Ԏ `   @*  0 `   @*B  s *޽h ? ̙33 Default Design 0 ^N0   (    0z z4CH 104: SYNTHESIS OF ASPIRIN AND OIL OF WINTERGREEN*54   0z0 z #Is it animal, vegetable, or mineral? Until the mid-1800s most scientists thought that all carbon compounds originated from plants and animals. As a result, organic chemistry was defined as the chemistry of carbon. In contrast, inorganic chemistry was defined as the chemistry of minerals.\$7+n  C FA.JosephWright-Alchemist@ H  0޽h ? ̙33___PPT10i.I6A+D=' = @B +r0 ^N0 qi(    0ez  a'ORGANIC CHEMISTRY AND FUNCTIONAL GROUPS((2(  0(0d Today s experiment is an example of organic chemistry. Organic molecules usually have very complicated structures. Therefore, organic chemists often use specific parts of molecules when they make other compounds. These parts are called functional groups. A functional group is an atom or group of atoms that defines the structure, physical properties, and chemical reactivity of a particular family of organic compounds. In today s experiment you will use different functional groups to synthesize aspirin (acetylsalicylic acid) from salicylic acid and acetic anhydride, and oil of wintergreen (methyl salicylate) from salicylic acid and methanol.<x_ $H  0޽h ? ̙33___PPT10i.?<PX&G+D=' = @B +0 ^N0  y(    0xzF0 c This is an esterification reaction. A phenol (the functional group of salicylic acid) reacts with an acid anhydride (the functional group of acetic anhydride) to make an ester (the functional group of acetylsalicylic acid).( #! L  C $A esterz *T  C ,Aanhydride0 DPV   0z  RTHE SYNTHESIS OF ASPIRIN(2^  C (Aasp3102"`R`& P  C (Aasp3101FN  C &Aphenolp 0" H  0޽h ? ̙33___PPT10i.I6A+D=' = @B +0 ^N0 >6(    0+B#style.visibility<*"%(D' =-6B'blinds(horizontal)*<3<*"D' =%(D' =%(DG' =4@BBB B%(D' =1:Bvisible*o3>+B#style.visibility<*%(D' =-6B'blinds(horizontal)*<3<*D' =%(D' =%(DG' =4@BBB B%(D' =1:Bvisible*o3>+B#style.visibility<*2u%(D' =-6B'blinds(horizontal)*<3<*2u+.0 ^N0 ` X  (    0z0 :,$@ 0 (A reaction mechanism is a detailed account of every valence electron during a reaction. The reaction mechanism for the catalytic esterification of salicylic acid and acetic anhydride has 5 steps. Use Lewis structures to predict the product of each step. What is the catalyst? H+. It is recycled during the reaction. It is not permanently created. And it is not permanently consumed.zl\  C &Astep1a"`   C &Astep1b"`\,$D0  C &Astep2a"` 0,$D0  C &A step2b"`\0,$D0  C &A step3a"`1  ,$D0  C &A step3b"`0\ ,$D0  C &A step4a"` 0 ,$D0  C &A step4b"` b2 ,$D0  C &Astep5a"` ,$D 0  C &Astep5b"` b,$D 0B  <Do ,$@ 0B  <Do @ ,$D 0H  0޽h ? ̙33##___PPT10#.I6A+ D#' = @B DU#' = @BA?%,( < +O%,( < +D' =%(D' =%(DG' =4@BBB B%(D' =1:Bvisible*o3>+B#style.visibility<*%(D' =-6B'blinds(horizontal)*<3<*D' =%(D' =%(DG' =4@BBB B%(D' =1:Bvisible*o3>+B#style.visibility<*%(D' =-6B'blinds(horizontal)*<3<*D' =%(D' =%(DG' =4@BBB B%(D' =1:Bvisible*o3>+B#style.visibility<*%(D' =-6B'blinds(horizontal)*<3<*D' =%(D' =%(DG' =4@BBB B%(D' =1:Bvisible*o3>+B#style.visibility<* %(D' =-6B'blinds(horizontal)*<3<* D' =%(D' =%(DG' =4@BBB B%(D' =1:Bvisible*o3>+B#style.visibility<* %(D' =-6B'blinds(horizontal)*<3<* D' =%(D' =%(DG' =4@BBB B%(D' =1:Bvisible*o3>+B#style.visibility<* %(D' =-6B'blinds(horizontal)*<3<* D' =%(D' =%(DG' =4@BBB B%(D' =1:Bvisible*o3>+B#style.visibility<* %(D' =-6B'blinds(horizontal)*<3<* D' =%(D' =%(DG' =4@BBB B%(D' =1:Bvisible*o3>+B#style.visibility<* %(D' =-6B'blinds(horizontal)*<3<* D' =%(D' =%(DG' =4@BBB B%(D' =1:Bvisible*o3>+B#style.visibility<*%(D' =-6B'blinds(horizontal)*<3<*D' =%(D=' =%(DG' =4@BBB B%(D' =1:Bvisible*o3>+B#style.visibility<*%(D' =-6B'blinds(horizontal)*<3<*DG' =4@BBB B%(D' =1:Bvisible*o3>+B#style.visibility<*%(D' =-6B'blinds(horizontal)*<3<*DG