Hi there. Could you please show a stepwise mechanism for the following: Please SHOW ALL STEPS so I can understand. Thanks! :)
Hi there. Could you please show a stepwise mechanism for the following: Please SHOW ALL STEPS...
Propose a stepwise mechanism for the synthesis of N,N-diethyl-m-toluamide (DEET). please show all steps! thanks (CH,CHy), WH -CH,CH) NHCr N(CH, CH,) SOCI -HCI CAM3 -5 CAM
5. Write the complete stepwise mechanism for this reaction. Show all electron flow with arrows and show all intermediate structures. (10 Points) CH, Br2 Br (or Cla) HI Br 7 6. Predict the major product for the following reactions PhCOM
provide the major organic product and show the detailed stepwise mechanism. Please show arrows. LTED 13:12 Raeford Yesterday 17:37 Edit Provide the major organic product AN O но NaOH TTI Arial 3 (120
please help Short Answer: (A) Draw all 3 steps of mechanism that gives the product 2-butene. You do not have to draw mechanisms for both products - just 2-butene (either cis or trans). Finally, clearly label each product below as the Hoffman or Zaitsev product. See Key Mechanism 7-5. ОН H2SO4 heat trans-2-butene 1-butene (C) Show ALL steps of the mechanism for the complete chlorination of 2 Cl2
Hi! Could you help me with this problem please 2 Another possible product of the E1 dehydration of 2-methylcyclohexanol is methylenecyclohexane (see structure below), but it is formed only in trace amounts Draw the reaction mechanism, including curved arrows as appropriate, for the formation of this product. Why is this product minor, rather than major?
please be clear and show the necessary steps. please use a legible writing. I really want to understand the process and mechanisms 2. Write the mechanism for the following reactions: a. the reaction of acetyl chloride with water to form acetic acid b. the reaction of acetyl bromide with methylamine to form N-methylacetamide 3. Write the mechanism in acid catalysis of the trans-esterification reaction of "methyl acetate" and ethanol.
PLEASE ANSWER ALL QUESTIONS Question 5 The reaction below occurs via SN2 and E2 reaction mechanisms. The question only requires you to address the E2 reaction only. For the E2 reaction: Use Newman projections to show the relationship between the leaving group and the beta-hydrogen on the carbon labeled with the asterisk ("). 1. If the leaving group and the beta-hydrogen on the carbon labeled with the asterisk (1) are not in the correct orientation, show the result of the...
Provide a stepwise mechanism for the formation of 2-[(3,4-dimethoxyphenyl)methylene]-2,3-dihydro-1H-inden-1-one from 3,4-dimethoxybenzaldehyde and 1-indanone. Please show all steps! This is a crossed aldol condensation. Thanks! Crossed aldol condensation of 3,4-dimethoxybenzaldehyde and l-indanone CHO CH,0 NaOH spolu co m ments CH,O CH,09 enolate formation OH -H,0 T dehydration CHO OH O CH,0 CHOA carbonyl addition CH,0 initial aldol product
can you please show all the steps (not just this) with every arrow and mechanisms and show exactly how to get to these states please? thank you so much. I just don't understand how to get actually get to these products (neutral form) H* (trace) heat + aos NH2 NaBH3CN or H2, metal cat (Pd/C, Ni, or Raney Ni)
Could someone answer this correctly for me please, explaining the mechanism. Thank you. 22) Write a detailed, stepwise mechanism to show formation of the major product from the reaction conditions shown below (this means draw the curved arrows). br sh BONUS (1 point): name the starting material following IUPAC nomenclature.