MS CHOUHAN|Exercise LEVEL-2 (SUBJECTIVE PROBLEMS)|1 Videos
ALDEHYDES AND KETONES
MS CHOUHAN|Exercise LEVEL-2|20 Videos
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{:(CH_2OH),(|),(C=O),(|),((CH_2 OH)_3),(|),(CH_2OH):} Total number of possible configuational stereo isomers
Reaction I : CH_(3)CH_(2)-underset(+N(CH_(3))_(3)OH^(-))(CH-CH_(3))overset("heat")to Product Reaction II : CH_(3)CH_(2)-underset(Br)underset(|)CH-CH_(3)overset(CH_(3)ONa)to Product Products are CH_(3)-CH=CH-CH_(3)(X) CH_(3)CH_(2)CH=CH_(2)(Y)
CH_(3)CH_(2)MgBr underset(H_(2)O)overset(CH_(3)CHO)rarr X overset(HBr)rarr Y . Write the product obtained when compound Y is subjected to dehydrohalogenation
C_(6)H_(5)CHO + HCN rarr C_(6)H_(5)CH(CN)OH . The product would be
CH_3-underset(OH)underset(|)CH-CH_2-CH_3 overset(Conc. H_2SO_4)to " Product(I) + Product(II)" What is not true regarding the products ?
CH_3 -CH_2 -underset( O) underset(||) C - CHO overset( NaBH_4) to Product (s) in the above reaction is (are)
(CH_(3))_(2)C=CH-CH_(3)overset(H^(+)//KMnO_(4))rarr Products in this reaction
Oxymercuration demercuration reacti on is process of addition H_2O according to Markownikoff's rule without any rearrangement . CH_3 - CH = CH_2 underset(NaBH_4. overset(odot)OH)overset(Hg(OAc)_2 . H_2O) to CH_3 - underset(OH)underset(|)CH=CH_3 Mechanism : Hg(OAc)_2 iffoverset(oplus)Hg(OAc) + Acoverset(odot)O Base overset(Ɵ)OH is used to neutralise H^(oplus) produced during the reaction : CH_3 - underset(CH_3)underset(|)overset(CH_3)overset(|)C-CH= CH_2 underset(NaBH_4, OH) overset(Hg(OAc)_2, CH_3OH)to "Product" :
MS CHOUHAN-ALCOHOL,ETHERS AND EPOXIDES-SUBJECTIVE PROBLEMS