diff --git a/CHEM Ch-12 Aldehydes, Ketones and Carboxylic acids.md b/CHEM Ch-12 Aldehydes, Ketones and Carboxylic acids.md new file mode 100644 index 0000000..6fa299c --- /dev/null +++ b/CHEM Ch-12 Aldehydes, Ketones and Carboxylic acids.md @@ -0,0 +1,621 @@ +# CHEM Ch-12 Aldehydes, Ketones and Carboxylic acids + +tags: #anki +- [ ] #todo Preliminary reactions +- [ ] #todo Merge all various methods of preparation +- [ ] #todo Do and add PYQs + +TARGET DECK +Raagaception's 12STD CBSE Deck::Chemistry +FILE TAGS +Raagaception_12STD::CHEM::Ch-12_aldehydes-ketones-carboxylic + +--- + +# aldehydes and ketones + +The general of structure of Aldehydes is
![](https://i.imgur.com/tsnMUdy.png)*(where $R$ = $\ce{H}$, alkyl or aryl)* + +The general of structure of Ketones is
![](https://i.imgur.com/UjowklB.png) *(where $R$ = alkyl or aryl)* + +The $\ce{C}$-atom of carbonyl group is ==$s p^{2}$== hybridised.. + + + +The $\ce{C}$-atom of carbonyl group forms ==three== $\sigma$ -bonds and ==one== $\pi$ -bond with $O$ atom. + + + +Carbonyl carbon with three atoms attached to it lie in a same plane with bond angle ==$120^{\circ}$ (trigonal coplanar structure)== and $\pi$ -electron cloud lies above and below of this plane. + + + +## preparation + +--- + +==![](https://i.imgur.com/KZ9aIEK.png)== ==![](https://i.imgur.com/rWTPm4t.png)== ==![](https://i.imgur.com/wvVahgl.png)== + + + + +==![](https://i.imgur.com/Ycnk3lH.png)== ==![](https://i.imgur.com/rWTPm4t.png)== ==![](https://i.imgur.com/2KoDpFY.png)== + + + +--- + +==![](https://i.imgur.com/w5I6EHk.png)== ==![](https://i.imgur.com/NwuNq3K.png)== ==![](https://i.imgur.com/hljtYn1.png)== + + + +==![](https://i.imgur.com/sFPftCr.png)== ==![](https://i.imgur.com/NwuNq3K.png)== ==![](https://i.imgur.com/2WTR3yT.png)== + + + +--- + +==![](https://i.imgur.com/VfzqiTi.png)== ![](https://i.imgur.com/vhPCEiF.png) ==![](https://i.imgur.com/71QAZ1D.png)== ==![](https://i.imgur.com/mvVMHSk.png)== ==![](https://i.imgur.com/pGyhhSQ.png)== + + + +==![](https://i.imgur.com/VfzqiTi.png)== ![](https://i.imgur.com/vhPCEiF.png) ==![](https://i.imgur.com/epCyunW.png)== + + + +==![](https://i.imgur.com/epCyunW.png)== ==![](https://i.imgur.com/mvVMHSk.png)== ==![](https://i.imgur.com/pGyhhSQ.png)== + + + +--- + +###### Give the reaction for Rosenmund reduction. +![](https://i.imgur.com/RX6INXW.png) ![](https://i.imgur.com/f7XsPDq.png) ![](https://i.imgur.com/y07z2xA.png) + + + +###### Name the reaction.
![](https://i.imgur.com/RX6INXW.png) ![](https://i.imgur.com/f7XsPDq.png) ![](https://i.imgur.com/y07z2xA.png) +Rosenmund reduction. + + + +==![](https://i.imgur.com/RX6INXW.png)== ==![](https://i.imgur.com/f7XsPDq.png)== ==![](https://i.imgur.com/y07z2xA.png)== + + + +--- + +==![](https://i.imgur.com/sTZOoz4.png)== ==![](https://i.imgur.com/846Ej4G.png)== ==![](https://i.imgur.com/TjlOL3u.png)== + + + +==![](https://i.imgur.com/sTZOoz4.png)== ==![](https://i.imgur.com/OiNcNjH.png)== ==![](https://i.imgur.com/BJ7mhr9.png)== + + + +###### Give the reaction for Stephen reduction. +![](https://i.imgur.com/sTZOoz4.png) ![](https://i.imgur.com/FIOrNPu.png) ![](https://i.imgur.com/lP6i1g7.png) + + + +###### Name the reaction.
![](https://i.imgur.com/sTZOoz4.png) ![](https://i.imgur.com/FIOrNPu.png) ![](https://i.imgur.com/lP6i1g7.png) +Stephen reduction. + + + +==![](https://i.imgur.com/sTZOoz4.png)== ==![](https://i.imgur.com/FIOrNPu.png)== ==![](https://i.imgur.com/lP6i1g7.png)== + + + +--- + +==![](https://i.imgur.com/6Ku4oxv.png)== ==![](https://i.imgur.com/JSDm2lN.png)== ==![](https://i.imgur.com/stRn4dU.png)== + + + +--- + + +###### Give the reaction for Gatterman-Koch reaction. +![](https://i.imgur.com/eWAZr4w.png) ![](https://i.imgur.com/RqkMuXR.png) ![](https://i.imgur.com/gYTrwne.png) + + + +###### Name the reaction.
![](https://i.imgur.com/eWAZr4w.png) ![](https://i.imgur.com/RqkMuXR.png) ![](https://i.imgur.com/gYTrwne.png) +Gatterman-Koch reaction. + + + +==![](https://i.imgur.com/eWAZr4w.png)== ==![](https://i.imgur.com/RqkMuXR.png)== ==![](https://i.imgur.com/gYTrwne.png)== + + + +--- + +###### Give the reaction for Friedel-Crafts acylation. +![](https://i.imgur.com/eWAZr4w.png)![](https://i.imgur.com/ApKtHrJ.png) ![](https://i.imgur.com/tFNC4xo.png) + + + +###### Name the reaction.
![](https://i.imgur.com/eWAZr4w.png)![](https://i.imgur.com/ApKtHrJ.png) ![](https://i.imgur.com/tFNC4xo.png) +Friedel-Crafts acylation. + + + +==![](https://i.imgur.com/eWAZr4w.png)== ==![](https://i.imgur.com/ApKtHrJ.png)== ==![](https://i.imgur.com/tFNC4xo.png)== + + + +--- + +==![](https://i.imgur.com/FQgFdct.png)== ![](https://i.imgur.com/8qghftd.png) ![](https://i.imgur.com/sjqtAnF.png) + + + +==![](https://i.imgur.com/FQgFdct.png)== ![](https://i.imgur.com/8qghftd.png) ![](https://i.imgur.com/SrCUiLR.png) + + + +==![](https://i.imgur.com/FQgFdct.png)== ![](https://i.imgur.com/gIb6yIJ.png) ![](https://i.imgur.com/sjqtAnF.png) + + + +==![](https://i.imgur.com/FQgFdct.png)== ![](https://i.imgur.com/gIb6yIJ.png) ![](https://i.imgur.com/SrCUiLR.png) + + + +![](https://i.imgur.com/FQgFdct.png) ![](https://i.imgur.com/8qghftd.png) ==![](https://i.imgur.com/Ombd9HW.png)== + + + +![](https://i.imgur.com/FQgFdct.png) ![](https://i.imgur.com/gIb6yIJ.png) ==![](https://i.imgur.com/Ombd9HW.png)== + + + +![](https://i.imgur.com/FQgFdct.png) ==![](https://i.imgur.com/jlda1CA.png)== ![](https://i.imgur.com/sjqtAnF.png) + + + +![](https://i.imgur.com/FQgFdct.png) ==![](https://i.imgur.com/jlda1CA.png)== ![](https://i.imgur.com/SrCUiLR.png) + + + +--- + +==![](https://i.imgur.com/DxD136H.png)== ==![](https://i.imgur.com/frJMR9e.png)== ==![](https://i.imgur.com/2I9T0o2.png)== + + + +==![](https://i.imgur.com/r66PNw5.png)== ==![](https://i.imgur.com/8tAoGkH.png)== ==![](https://i.imgur.com/IRsglQD.png)== + + + +--- + +###### Give the reaction for Etard reaction. +![](https://i.imgur.com/VGPRwLB.png) ![](https://i.imgur.com/qX0SeKG.png) ![](https://i.imgur.com/q7cU2St.png) + + + +###### Name the reaction.
![](https://i.imgur.com/VGPRwLB.png) ![](https://i.imgur.com/qX0SeKG.png) ![](https://i.imgur.com/q7cU2St.png) +Etard reaction. + + + +==![](https://i.imgur.com/VGPRwLB.png)== ==![](https://i.imgur.com/qX0SeKG.png)== ==![](https://i.imgur.com/q7cU2St.png)== + + + +--- + +==![](https://i.imgur.com/VGPRwLB.png)== ==![](https://i.imgur.com/jdp6Ary.png)== ==![](https://i.imgur.com/q7cU2St.png)== + + + +--- + +## physical properties + +==Lower== *(higher/lower?)* members of aldehydes and ketones (up to $C _{10}$ ) are colourless, volatile liquids with the exception of ==formaldehyde *(which is gas at ordinary temperature)==*. + + + +==Higher== *(higher/lower?)* members of aldehydes and ketones are solids with fruity odour. + + + +==Lower== *(higher/lower?)* aldehydes have ==unpleasant== odour. + + + +Ketones have ==pleasant== odour. + + + +###### Explain why : "The boiling points of aldehydes and ketones are higher than hydrocarbons and ethers of comparable molecular masses" +The boiling points of aldehydes and ketones are higher than hydrocarbons and ethers of comparable molecular masses due to **weak dipole-dipole interactions**. + + + +The boiling points of aldehydes and ketones are ==higher== than hydrocarbons and ethers of comparable molecular masses. *(higher/lower?)* + + + +The boiling points of hydrocarbons and ethers are ==lower== than aldehydes and ketones of comparable molecular masses. *(higher/lower?)* + + + +###### Explain why : "The boiling points of aldehydes and ketones are lower than alcohols of similar molecular masses" +Their boiling points are lower than those of alcohols of similar molecular masses, due to **absence of intermolecular hydrogen bonding**. + + + +The boiling points of aldehydes and ketones are ==lower== than alcohols of similar molecular masses. *(higher/lower?)* + + + +The boiling points of alcohols are ==higher== than aldehydes and ketones of similar molecular masses. *(higher/lower?)* + + + +###### Explain why : "Among isomeric aldehydes and ketones, ketones have slightly higher boiling points" +Among isomeric aldehydes and ketones, ketones have slightly higher boiling points due to the **presence of two electron releasing alkyl groups**, which make carbonyl group more polar. + + + +The boiling points of isomeric ketones are ==slightly higher== than isomeric aldehydes. *(higher/lower?)* + + + +The boiling points of isomeric aldehydes are ==slightly lower== than isomeric ketones. *(higher/lower?)* + + + +--- + +###### Explain why : "Lower members of aldehydes and ketones (up to $C _{4}$ ) are soluble in water" +Lower members of aldehydes and ketones (up to $C _{4}$ ) are soluble in water due to **H-bonding between polar carbonyl group and water**. + + + +==Lower== members of aldehydes and ketones are soluble in water. *(higher/lower?)* + + + +The solubility of aldehydes and ketones ==decreases== with ==increase== in molecular weight. + + + +The solubility of aldehydes and ketones ==increases== with ==decrease== in molecular weight. + + + +###### Explain why : "Aromatic aldehydes and ketones are much less soluble than corresponding aliphatic aldehydes and ketones" +Aromatic aldehydes and ketones are much less soluble than corresponding aliphatic aldehydes and ketones due to **larger benzene ring**. + + + +The solubility of aromatic aldehydes and ketones are ==much lower== than corresponding aliphatic aldehydes and ketones. *(higher/lower?)* + + + +The solubility of aliphatic aldehydes and ketones are ==much higher== than corresponding aromatic aldehydes and ketones. *(higher/lower?)* + + + +All carbonyl compounds are ==fairly soluble== in organic solvents. *(soluble/insoluble?)* + + + +--- + +## chemical properties + +==![](https://i.imgur.com/x4Cv9F2.png)== ==![](https://i.imgur.com/7umnipy.png)== ==![](https://i.imgur.com/riKx7kt.png)== + + + +==![](https://i.imgur.com/x4Cv9F2.png)== ==![](https://i.imgur.com/faJBwBQ.png)== ==![](https://i.imgur.com/mW7IhUG.png)== + + + +==![](https://i.imgur.com/x4Cv9F2.png)== ==![](https://i.imgur.com/trrlxZw.png)== ==![](https://i.imgur.com/F5vHzBj.png)== + + + +==![](https://i.imgur.com/x4Cv9F2.png)== ==![](https://i.imgur.com/Z7Xqyk9.png)== ==![](https://i.imgur.com/K1jmvts.png)== + + + +--- + +==![](https://i.imgur.com/x4Cv9F2.png)== ==![](https://i.imgur.com/ufIB9z9.png)== ==![](https://i.imgur.com/QMIEqoD.png)== ==![](https://i.imgur.com/ufIB9z9.png)== ==![](https://i.imgur.com/M7YyESx.png)== + + + +==![](https://i.imgur.com/x4Cv9F2.png)== ==![](https://i.imgur.com/ufIB9z9.png)== ==![](https://i.imgur.com/QMIEqoD.png)== + + + +==![](https://i.imgur.com/QMIEqoD.png)== ==![](https://i.imgur.com/ufIB9z9.png)== ==![](https://i.imgur.com/M7YyESx.png)== + + + +--- + +==![](https://i.imgur.com/x4Cv9F2.png)== ==![](https://i.imgur.com/muORCT9.png)== ==![](https://i.imgur.com/NCuwW8c.png)== + + + +--- + +==![](https://i.imgur.com/x4Cv9F2.png)== ==![](https://i.imgur.com/O6JzGan.png)== ==![](https://i.imgur.com/x1XTvTe.png)== + + + +==![](https://i.imgur.com/x4Cv9F2.png)== ==![](https://i.imgur.com/IQ1QwQT.png)== ==![](https://i.imgur.com/ETKVAZQ.png)== + + + +==![](https://i.imgur.com/x4Cv9F2.png)== ==![](https://i.imgur.com/EzMmtc3.png)== ==![](https://i.imgur.com/3GEwr0w.png)== + + + +==![](https://i.imgur.com/x4Cv9F2.png)== ==![](https://i.imgur.com/zJGpdge.png)== ==![](https://i.imgur.com/bkPammZ.png)== + + + +==![](https://i.imgur.com/x4Cv9F2.png)== ==![](https://i.imgur.com/zWkv27m.png)== ==![](https://i.imgur.com/RS221lS.png)== + + + +==![](https://i.imgur.com/x4Cv9F2.png)== ==![](https://i.imgur.com/iLtnnLz.png)== ==![](https://i.imgur.com/SwDHKKr.png)== + + + +--- + +==![](https://i.imgur.com/qMJhuoJ.png)== ==![](https://i.imgur.com/0Tlg3AZ.png)== ==![](https://i.imgur.com/zW46LVW.png)== + + + +###### Give the reaction for Silver mirror test. +![](https://i.imgur.com/qMJhuoJ.png) ![](https://i.imgur.com/Ls1eRpx.png) ![](https://i.imgur.com/BPNCF6o.png) + + + +==![](https://i.imgur.com/qMJhuoJ.png)== ==![](https://i.imgur.com/Ls1eRpx.png)== ==![](https://i.imgur.com/BPNCF6o.png)== + + + +###### Give the reaction for Fehling's solution test. +![](https://i.imgur.com/qMJhuoJ.png) ![](https://i.imgur.com/48ukEZO.png) ![](https://i.imgur.com/8eG6886.png) + + + +==![](https://i.imgur.com/qMJhuoJ.png)== ==![](https://i.imgur.com/48ukEZO.png)== ==![](https://i.imgur.com/8eG6886.png)== + + + +###### Give the reaction for Benedict's solution test. +![](https://i.imgur.com/qMJhuoJ.png) ![](https://i.imgur.com/Mc1aCyZ.png) ![](https://i.imgur.com/BYMNcC3.png) + + + +![](https://i.imgur.com/qMJhuoJ.png) ==![](https://i.imgur.com/Mc1aCyZ.png)== ![](https://i.imgur.com/BYMNcC3.png) + + + +==![](https://i.imgur.com/qMJhuoJ.png)== ![](https://i.imgur.com/MT3oVN0.png) ==![](https://i.imgur.com/BYMNcC3.png)== + + + +==![](https://i.imgur.com/qMJhuoJ.png)== ![](https://i.imgur.com/2eoS6Q6.png) ==![](https://i.imgur.com/BYMNcC3.png)== + + + +--- + +![](https://i.imgur.com/AJwXCk5.png) ==![](https://i.imgur.com/RaR81wI.png)== ![](https://i.imgur.com/v2tGlSC.png) + + + +==![](https://i.imgur.com/AJwXCk5.png)== ![](https://i.imgur.com/7BV0rur.png) ==![](https://i.imgur.com/v2tGlSC.png)== + + + +==![](https://i.imgur.com/AJwXCk5.png)== ![](https://i.imgur.com/jFfQGkX.png) ==![](https://i.imgur.com/v2tGlSC.png)== + + + +==![](https://i.imgur.com/AJwXCk5.png)== ![](https://i.imgur.com/4Im3z20.png) ==![](https://i.imgur.com/v2tGlSC.png)== + + + +==![](https://i.imgur.com/AJwXCk5.png)== ![](https://i.imgur.com/l4m3Xet.png) ==![](https://i.imgur.com/v2tGlSC.png)== + + + +==![](https://i.imgur.com/AJwXCk5.png)== ![](https://i.imgur.com/9jmOZHS.png) ==![](https://i.imgur.com/v2tGlSC.png)== + + + +--- + +###### Give the reaction for Clemmensen reduction. +![](https://i.imgur.com/AJwXCk5.png) ![](https://i.imgur.com/QafcLDn.png) ![](https://i.imgur.com/27cadK3.png) + + + +###### Name the reaction.
![](https://i.imgur.com/AJwXCk5.png) ![](https://i.imgur.com/QafcLDn.png) ![](https://i.imgur.com/27cadK3.png) +Clemmensen reduction. + + + +###### Give the reaction for Wolff–Kishner reduction. +![](https://i.imgur.com/AJwXCk5.png) ![](https://i.imgur.com/RjE5cX0.png) ![](https://i.imgur.com/27cadK3.png) + + + +###### Name the reaction.
![](https://i.imgur.com/AJwXCk5.png) ![](https://i.imgur.com/RjE5cX0.png) ![](https://i.imgur.com/27cadK3.png) +Wolff–Kishner reduction. + + + +![](https://i.imgur.com/AJwXCk5.png) ==![](https://i.imgur.com/rJKaE15.png)== ![](https://i.imgur.com/27cadK3.png) + + + +==![](https://i.imgur.com/AJwXCk5.png)==![](https://i.imgur.com/QafcLDn.png) ==![](https://i.imgur.com/27cadK3.png)== + + + +==![](https://i.imgur.com/AJwXCk5.png)== ![](https://i.imgur.com/66cJ2pY.png) ==![](https://i.imgur.com/27cadK3.png)== + + + +==![](https://i.imgur.com/AJwXCk5.png)== ![](https://i.imgur.com/RjE5cX0.png) ==![](https://i.imgur.com/27cadK3.png)== + + + +--- + +![](https://i.imgur.com/vzcBtiO.png)![](https://i.imgur.com/LMad3xP.png)==![](https://i.imgur.com/lTTuA5l.png)== + + + +![](https://i.imgur.com/TErYXcg.png) ![](https://i.imgur.com/LMad3xP.png) ==![](https://i.imgur.com/qciUeaD.png)== + + + +--- + +==![](https://i.imgur.com/vPjLJ1B.png)== ==![](https://i.imgur.com/HvJGAar.png)== ==![](https://i.imgur.com/ujX0jLn.png)== ==![](https://i.imgur.com/rZkXdKy.png)== ==![](https://i.imgur.com/MRwM1hj.png)==

*(Aldol Condensation reaction)* + + + +==![](https://i.imgur.com/OArbc6E.png)== ==![](https://i.imgur.com/HvJGAar.png)== ==![](https://i.imgur.com/0Coyvlj.png)== + + + +==![](https://i.imgur.com/0Coyvlj.png)== ==![](https://i.imgur.com/rZkXdKy.png)== ==![](https://i.imgur.com/VGRYFmT.png)== + + + +--- + +###### What is intramolecular aldol condensation? +Intramolecular aldol condensation takes place in diketones and gives rise to cyclic products. + + + +###### What is crossed aldol condensation? +Crossed aldol condensation is carried out between two different aldehydes and/or ketones, and if both of them contain $\alpha$ -hydrogen atoms, it gives a mixture of four products. + + + +--- + +###### Give the reaction for Cannizzaro reaction. +![](https://i.imgur.com/UMGCia9.png) ![](https://i.imgur.com/z4FWfaI.png) ![](https://i.imgur.com/Eb1HuFp.png) +*(shown by aldehydes which do not have an $\alpha$ -hydrogen atom)* + + + +###### Name the reaction.
![](https://i.imgur.com/k2cUdZa.png) ![](https://i.imgur.com/z4FWfaI.png) ![](https://i.imgur.com/lvsTydE.png) +Cannizzaro reaction. + + + +==![](https://i.imgur.com/k2cUdZa.png)== ==![](https://i.imgur.com/z4FWfaI.png)== ==![](https://i.imgur.com/lvsTydE.png)== + + + +--- + +###### Give the reaction for Crossed Cannizzaro reaction. +![](https://i.imgur.com/H9zGbQj.png) ![](https://i.imgur.com/rZkXdKy.png) ![](https://i.imgur.com/pU8k7Io.png) + + + +###### Name the reaction.
![](https://i.imgur.com/H9zGbQj.png) ![](https://i.imgur.com/rZkXdKy.png) ![](https://i.imgur.com/qQHfkD1.png) +Crossed Cannizzaro reaction. + + + +==![](https://i.imgur.com/H9zGbQj.png)== ==![](https://i.imgur.com/rZkXdKy.png)== ==![](https://i.imgur.com/qQHfkD1.png)== + + + +###### What is Intramolecular Cannizzaro reaction? +Intramolecular Cannizzaro reaction is given by dialdehydes having no $\alpha$ -hydrogen atoms. + + + +--- + +Aromatic aldehydes and ketones undergo ==electrophilic== substitution at the ring in which the ==carbonyl== group acts as a ==deactivating and meta directing== group. + + + +###### What happens when Schiff's reagent is added to aldehydes? +Appearance of pink colour. + + + +###### What happens when Schiff's reagent is added to ketones? +No colour. + + + +###### What happens when Fehling's solution is added to aldehydes? +Appearance of red precipitate. + + + +###### What happens when Fehling's solution is added to ketones? +No precipitate. + + + +###### What happens when Tollen's reagent is added to aldehydes? +Appearance of Silver mirror. + + + +###### What happens when Tollen's reagent is added to ketones? +No Silver mirror. + + + +###### What happens when $2,4-$Dinitrophenylhydrazine is added to aldehydes? +Evolution of orange-yellow or red well defined crystals, with melting points characteristic of individual aldehydes. + + + +###### What happens when $2,4-$Dinitrophenylhydrazine is added to ketones? +Evolution of orange-yellow or red well defined crystals, with melting points characteristic of individual ketones. + + + +--- + +# carboxylic acids + +In carboxylic acids, the bonds to the carboxyl carbon lie in one plane and are separated by about ==$120^{\circ}$==. + + + +###### Explain why : "Carboxylic carbon is less electrophilic than carbonyl carbon " +The carboxylic carbon is less electrophilic than carbonyl carbon because of the possible** resonance structure**.
![](https://i.imgur.com/tMjMBtY.png) + + + +The carboxylic carbon is ==less== electrophilic than carbonyl carbon. *(more/less)* + + + +The carbonyl carbon is ==more== electrophilic than carboxylic carbon. *(more/less)* + + +