Predict the products of the following reactions. CH3 CH3 CH CH2 -NH2 -CH2 + H₂O CH3 + H₂O CH2 N CH3 1 1 1 CH2 + HCI CH3 NH2 CH2 CH3 + HCI CH3 CH3 CH3 OH + CH2 CH3 NH2 CH2 CH3 CH3 HO CH2 CH3
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- What is/are the product(s) of the following reaction? Assume the reaction can yield some product(s). CH3CH₂OH + CH₂CH₂ CH₂CH₂OH CH3CH₂CH₂CH₂OCH₂CH₂CH₂CH3 CH3CH₂OCH₂CH₂CH₂CH3 CH3CH₂OCH₂CH3 H3O+ All of the above.Predict the products of the following reactions. CH3CH2CH2CH2C‚N + DIBAL-H, then H3O+Predict the major products of this reaction. x Cl₂ hv ?
- Predict the major products of the following reaction. O H₂O+Predict the major products of the following reactions. the tosylate of cyclohexylmethanol + excess NHThe products in the following reaction are incorrect, briefly explain why the products are incorrect. oo OH + CH3CH3NHCH₂CH3 H₂C CH₂ CH3 + H₂O
- Select the major product of the following reactions. OIV Oll OV 01 IV FeCl3 Cl ? II III VPredict the major product of the following sequence of reactions. OH 1) PBгg 2) Mg ? 3) CH₂OH OH OCH3When 2,2-dimethylcyclohexanol is treated with acid, 1,2-dimethylcyclohexene and iso- propylidenecyclopentane are the products obtained. Draw a detailed mechanism that explains this result. CH3 H3O+ CH3 CH3 CH3 OH CH3 CH3 2,2-dimethyl- cyclohexanol 1,2-dimethyl- isopropylidene- cyclopentane cyclohexene
- Predict the products for each of the following reactions and propose a mechanism that explains the formation of each product.In EAS bromination reactions, a -NHCOCH3 substituent on the aromatic ring is: O an activator and an o,p-director. O a deactivator and a m-director. an activator and a m-director. NHCOCH3 catalyzes the 1,2 addition of bromine across the double bond O a deactivator and an o,p-director.Give major products of the reactions HCI HO (1) NaH (2) CH3CH2CI (1) XS NBS (2) CH3CH2CI, AICI3 PHCH2NH2 H30*