trans-1-ethyl-2-isopropylcyclohexane Drag the appropriate labels to their respective targets. Note: not all labels will be used. H CH3 CH₂CH₂ Submit Request Answer CH(CH3)2 CH(CH3)2 Reset Help

Help find major products for each step

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.

Draw the elimination products only for each reaction below. Label any alkene that would be formed predominantly as MAJOR. H3C Br CH3 OH H3C CH3 OH CH3 H.C Br Br OH CH3 H3C H3C CH3

Please help me with a drawn mechanism for the reaction shown.

draw and explain the mechanism of this reaction OH CH₂ PhCOCI in py CH3 KOH in py 3 C OH H₂SO, in 0000 CH, CON

Provide the necessary reagents next to the arrows.

Which of the following is not a product of this elimination reaction?  (C6H5- is a benzene ring)              Cl  CH3                         |     | CH3CH2CH2-CH-CH-C6H5                 +          CH3CH2OH               →                     CH3                               |  CH3CH2CH=CH-CH-C6H5                      CH2                                 ||  CH3CH2CH2CH2-C-C6H5                         CH3                                 |  CH3CH2CH2CH2-C=C6H5                       C6H5                                 |  CH3CH2CH2CH2-C=CH2                         CH3                                |  CH3CH2CH2CH=C-C6H5

Please answer BOTH questions, thanks so much!

The reaction of methylpropene with HBr in ether gives one of the two products below as the major product. Br HBr Br ether Product A Product B Product would have a higher energy transition state for the formation of the intermediate leading to it. O A O B O Both products would have the same transition state.