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- Reaction of 2-methyl-2-pentene with reagent is regioselective. Draw a structural formula for the product of reaction and account for the observed regioselectivity. Q.) H2O in the presence of H2SO4Reaction of 2-methyl-2-pentene with reagent is regioselective. Draw a structural formula for the product of reaction and account for the observed regioselectivity. Q.) Br2 in H2OLDA/THF, 78°Clongrightarrow Predict the major product of the following a- halogenation/a - alkylation reactions under the given reaction conditions.
- Reaction of 2-methyl-2-pentene with reagent is regioselective. Draw a structural formula for the product of reaction and account for the observed regioselectivity. Q.) HIReaction of 2-methyl-2-pentene with reagent is regioselective. Draw a structural formula for the product of reaction and account for the observed regioselectivity. Q.) HBrWrite out all the isomers of the compound with molecular formula C4H10O . Select the normal/ primaryisomer and treat it with conc. H2SO4 and heat. Identify the reaction and give the product ‘A’ from it. 2. When ‘A’ is treated with HBr in the presence of a peroxide, give the name and structure of the product.
- β-ocimene is a pleasant smelling hydrocarbon found in the leaves of a certain herbs. It has a molecular formula C10H16 and a UV absorption λmax 232nm. On hydrogenation with a palladium catalyst, 2,6-dimethyloctane is obtained. Ozonolysis β-ocimene followed by the treatment with zinc and acetic acid produces the following fragments:When 3-methyl-1-butene is reacted with 9-borabicyclo[3.3.1]nonane, the "1-ol" product is formed. What is the detailed reactin scheme for the transformation? Describe the purification procedure.The reaction of 2-ethyl-1-pentene with Br2, with H2 + Pd/C, or with R2BH/THF followed by aqueous HO- + H2O2 leads to a racemic mixture. Explain why a racemic mixture is obtained in each case.
- Compound X, C7H15Cl, is a chiral product of the radical chlorination of 2-methylhexane.Base-promoted E2 elimination of X gives a single product.What is the structure of X?Butanone is formed when an alkyne is passed through a dil sol of H2SO4at 330K in presence of mercuric sulphate. Write the possible structure of the alkyne.What alkene would yield 2,2-dimethoxycyclopentane-1,3-dicarbaldehyde on treatment with O3 followed by (CH3)2S?