From e2310d148becdee67eaaacdae5fb7982db19b67b Mon Sep 17 00:00:00 2001
From: Raagaception <72780589+Raagaception@users.noreply.github.com>
Date: Wed, 19 May 2021 21:53:48 +0530
Subject: [PATCH] Add files via upload
Testing out the pull/push system.
---
...Aldehydes, Ketones and Carboxylic acids.md | 621 ++++++++++++++++++
1 file changed, 621 insertions(+)
create mode 100644 CHEM Ch-12 Aldehydes, Ketones and Carboxylic acids.md
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)*
+
+
+