In presence of h2so4, protonation occours at double bond and form tertiary carbocation (more stable compare to primary carbocation). Then h2o attack to this carbocation and form 2,6,6-trimethyl -2-heptanol.
Correct option: b)2,6,6-trimethyl-2-heptanol
IUPAC name of the compound is 3-chloro-6-cyclopropane benzaldehyde.
What is the major product that results when the following alkene is treated water and a...
formulas of all chloro that u when treated with KOH to give the following alkene as the major product. . Do not show stereochemistry in other cases. . Separate structures with + signs from the drop-down menu. ChemDoodle OWLv2 I Onine t are two dias s of 3-b ethoxide in xene as the major diastereomer gives the E alkene, and the other gives the Zalkene. Which diastereomer gives the E alkene? Me Me Me Br Me Et Et Et Following...
Draw the expected major organic product that results when
3,3-dimethyl-1-butene is treated with br2 in methanol
Draw the expected major organic product that results when 3,3-dimethyl-1-butene is treated with Br_2 in methanol.
Draw the structure of the major product which results when the diene shown is treated with HBr at -80°C. CH3 CH3 Draw the molecule on the canvas by choosing buttons from the Tools (for bonds), Atoms, and Advanced Template toolbars. The single bond is active by default. 1. H: 120 EXPONE H + с N o S CI Br Marvin JS 1 by ChemAxon P
Provide the structure of the major organic product that results when 2-butyne is treated with HgSO_4H_2SO_4 in water. Draw the molecule on the canvas by choosing buttons from the Tools (for bonds), Atoms, and Advanced Template toolbars. The single bond is active by default.
What is the major organic product that results when 1-heptyne is treated with 2 equivalents of HBr
2. (a) When the alkene below is treated with HCI, the major product obtained has the chloride on the less substituted carbon. Draw a mechanism for this reaction and provide an explanation for the observed regiochemistry. HCI (b) Provide a mechanism for the following transformation. НBr но- Br (c) Provide a mechanism for the following transformation 2 Он
27. Draw all likely alkene products in the following reaction and circle the product you expect to predominate. Br CHS (CH),CO K* (CH),COH 28. Predict the major product of the reaction shown below. OH H2PO, heat A. 2,3-dimethyl-2-butene B. 2,3-dimethyl-1-butene C. 3,3-dimethyl-1-butene D. None of the above 29. Draw all likely products of the following reaction and circle the product you expect to predominate. CH3 H2SO HO heat 30. Propose a detailed, step-by-step mechanism for the reaction pathway shown below....
Provide the major organic product(s) that results when benzene is treated with the following sequence of reagents: 1. HNO3, H2SO4 2. Br2, FeBr3
13. What is the major product in the following 14. The IUPAC name of the following compound is: a) 2,3-dimethyl-5-hexyne b) 4,5-dimethyl-1-hexyne c) 2,3-dimethyl-2-hexyne d) 5,6-dimethyl-2-heptyne 15. What is the major product in the following reaction? 1. NaNH2/NH 2. CHyBr NH2 -NH CHs B. CH2 CH3 CH3
8. Provide the major organic product which results when PhCH2CH2CO2H is treated with 2 eq. butyllithium followed by H30+. 9. Provide the major organic product which results when (CH3)2CHCH2CH2COCI is treated with LIAIH[OC(CH3)313-