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carboxylic acid altern

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Question
Answer
acyl halide   OH replaced by X  
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anhydride   OH replaced by OCOR  
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amide   Oh replaced by NH2  
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ester   OH replaced by OR  
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naming acyl haldes   change "ic acid" "yl acid"  
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Carboxylic acid + thionyl Chloride (SOCl2)or PCL3 or PBr3   acyl chloride  
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acyl chloride + h2O   forms back carboxylic acid  
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acyl chlroide + alcohol (ROH)   forms ester R-C=O \OR  
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acyl chlorides + ammonia (NH3)   forms amide R-C=O \NH2  
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aromatic substitution   Friedel craft acylation  
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wats friedel craft   aromatic + acid chloride with AlCl3  
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results of friedel craft   benzene-R-C=O \R  
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acid halide + H2 in Pd/BaSO4 (quinoline)   halide replaced by H  
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anhydride   without water; 2 acid bonding and removing water  
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gen form for anhydride   R-C=O \O-C=O \R  
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acid chloride + carboxylate salt ( R-C=O \O-   halide is lost and anhydride formed  
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dioic acid + heat   cyclic anhydride  
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anhydrydes + water   2 carboxylic acids - molecule splie adding OH to one and H to O  
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ammonia (NH3) + anhydride   mol splits forming carboxylate attached to NH4 -forms amide  
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anhydride + alcohol   mol splits and adds RO from alcohol to one and H to the O in the second - ester + carboxylic acid  
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anhydride + benzene in friedel craft( AlCl3)   splits anhydride and attaches R-C=O to benzene + carboxylate  
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amide gen formula   R-C=O \NR2  
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formation of amide   acid chlorides with amine (prim n sec) or anhydride with ammonia  
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amide+ H2O in acid   NR2 replaced by OH to form carboxylic acid  
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hoffman rearrangement (BrO-)   amide to primary amine ( loses carbonyl)  
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BrO- + amide   H2NR ( primary amine); Hoffman rerarrangement  
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amide + LAH   loses =O to form amine  
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gen formula for ester   RC=O \OR  
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synthesis of ester   acid + alcohol  
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naming ester   alkyl alkanoates  
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ester + h2o   H adds to =O forming OH and H adds to the other O splitting the ester - carboxylic acid and alcohol  
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ester + ammonia   adds H to O splitting the ester NH2 adds to carbonyl section - amide + alcohol  
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ester + alcohol   displaces the OR by adding H and adds the alcohols OR to the C=O grp - new ester + alcohol ( transesterification)  
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Grignard reagent (RMgBr) + ester   OR is replaced by the R grp - forms ketone  
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LAH + ester   - removes =O and adds H to the other O prim alcohol  
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ester + NaBH4   doesnt produce prim alchols  
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