please help Draw the mechanism for the transformation below. Be sure to draw all resonance structures...
5. (8 pt) Write a mechanism for the reaction shown below. Be sure to draw all intermediates and BOTH the 1,2- and 1,4-addition products for the reaction. Indicate which product is the THERMODYNAMIC PRODUCT and which is the KINETIC PRODUCT. HBr
Draw the mechanism for the following transformation. Include all relevant resonance structures. Show the movement of electrons with arrows. Draw the mechanism for the following transformation. Include all relevant resonance structures. Show the movement of electrons with arrows. (14 points) Pro excess HBr Br
Draw a plausible mechanism for the reaction shown below, being sure to show all intermediates, charges and resonance structures 4. Draw a plausible mechanism for the reaction shown below, being sure to show all intermediates, charges and resonance structures. (12 points) O CH3NH2O OH DCC
1. Please draw all resonance structures (if there are any, not all structures may have resonance structures) for the carbocations A-E (make sure you use resonance arrows (<->). Then circle the carbons that can react with a nucleophile in a SN1-type reaction.
Draw a detail arrow pushing mechanism for the following reaction. Also show the resonance structures of the intermediate whenever appropriate. HNO3/H2SO4 NO2 b)
Draw a detail arrow pushing mechanism for the following reaction. Also show the resonance structures of the intermediate whenever appropriate. -OH 50% H2SO4 Heat OR
1) Provide a detailed electron pushing mechanism for the below transformation. Show ALL relevant resonance structures to help explain why the para product is the major organic product. (Note: your electron pushing mechanism should include formation of the electrophile) (4 points) Cl AICl3
сн, Нас 12-addition products (direct addition) CH2 CH3 Н,с Н-с CH CI HCI CH2 Cн Н.с 1,4-addition products (conjugate addition) Cн CH3 Нас Н.С CI Electrophilic addition to an alkene proceeds via Markovnikov regiochemistry due to the formation of the more stable carbocation intermediate. In the case of conjugated dienes, that is dienes that are separated by one sigma bond, the carbocation that is formed is stabilized additionally by resonance. Addition of the nucleophile to the carbocation intermediate can therefore...
Klein, Organic Chemistry, 3e Help System Announcements Integrated Problem 07.89 Propose a mechanism for the following transformation: OH Step 1 Correct. Step 1 of the mechanism is a proton transfer step. Draw step 1 of the mechanism for the formation of this product. Include lone pairs ar the mechanism. OH HC Сн, en.wileyplus.com Joint Commission Amazon.com - Priceline.com TripAdvisor imported From Youtube to MP3 M Mathway trgono S Klein, Organic Chemistry, 3e Help System Announcements PRINTER VERSION BACK NEXT Step...
Draw the major 1.2- and 1,4-addition products obtained in the reaction shown. Assume that both are derived from the most stable carbocation intermediate + HBr • You do not have to consider stereochemistry • You do not have to explicitly draw Hatoms • If the 1,2- and 1,4- addition products are the same due to symmetry, only draw one structure. • Draw one structure per sketcher. Add additional sketchers using the drop down menu in the bottom right corner •...