need help with the mechanism must include all steps and show all
curly arrows and workings.
need help with the mechanism must include all steps and show all curly arrows and workings....
Need Help. Will Rate If Complete.
1) NaoEt, EtOH Br 2) O 3) H30+ / A. 1) NaoEt, EtOH (s) ar 2) Y Br 3) Hz0+ / A 1) NaOme/MeOH ~ Br OMe 3) Hz0+/A. 1) NaOEt, EtOH 2) V Br 3) NaOEt, EtOH COOEt 5) H30+/A Robinson Annulation NaoEt, EtOH/A come lui OMe 28- The following molecules can be formed by either: Michael Reaction; Enamine Acylation; Acetoacetic Ester Synthesis; Michael Addition; Malonic Ester Synthesis; Robinson Annulation; Aldol Condensation; Claisen...
What are the products? Include all lone pairs, mechanism arrows,
and steps. Include an acidic aqueous work-up at the end of the
reaction.
NEt CI он CH,Cь rt, 30 min O2N
For the mechanism, show all the steps with multiple reaction
arrows, electron arrows, formal charges, etc.
CONCEPT QUESTIONS Predict the Product. Provide the stable organic product(s) for the reactions below. 1. Mgº, CH3CH2OCH,CH3 2. CO2 (g) 3. H20, HCI 1. MgBr (1eq.) 2. H20, HCI Mechanism. Using ChemDraw, provide the complete mechanism for the following transformation. You must include appropriate arrows, intermediates, and formal charges. 1. MgCI 2. H20, HCI
Draw a plausible mechanism??? help please!
1) Making sure to show all steps and arrows, draw a plausible mechanism for the transformation show below. (10 points) + HBr
2. Provide the complete mechanism (curved arrows) to show how the product is formed. Include all lone pairs, formal charges, curved arrows, intermediates, and products. You do not need to draw the structures of transition states. If there is a carbocation rearrangement and/or a proton transfer, be sure to include it (them) in your mechanism. (Remember to start by drawing all ionic compounds as ions/drawing out the structure of all reagents, and drawing in all lone pairs.) HCI 3. Which...
need help with all practice test questions 5-12
5. Suggest a structure for the compound, CHO, which gives this proton NMR spectrum. (4 points) PPM AREA 4 6. Which isomer gives the carbon-13 NMR spectrum shown? (2 points) 100 160 - 80 PPM 140120 60 40 20 7. Add the intermediate and draw all curly arrows to complete this reaction mechanism. (6 points) oo ocн, ОСН 8. Draw a major product of each of the following reactions. (3 points each)....
please show all steps with necessary mechanism arrows
1. Provide the starting specific nucleophile and electrophile that would result in each of the following molecules using an SN2 reaction. Do consider the ABC and provide the specific reagent necessary. (2 points) Me HH MeMe Me I wyn Me Me 2. Provide a detailed retrosynthesis and synthesis of the following compound from the indicated starting material. All atoms of the target must come from the indicated starting materials. You may use...
please show all steps including each mechanism (arrows) and
also if SN1 has any rearrangements of carbocation intermediate
through a hydride shift and/or methyl shift. DO NOT NEED
ELIMINATION. ONLY SUBSTITUTION.
Sy1/E1 versus S2/E2 Learning Checks Draw the major organic substitution and/or elimination products in the following reactions. If no reaction is possible, write “No Reaction". Substitution Product(s) Elimination Product(s) 2) 2) OH BrCH K* -Ot-Bu NaOCH н"Сн, сн,он нсн, Ph NaOCH Br H CH3OH CH NaOCH NaOH T.CH, I...
Draw a detailed mechanism for the following reactions. Include
all steps with arrows and lone pairs.
6 Hea ㅓ t o 0 0 メou 1.soek 1. SOClz
6 Hea ㅓ t o 0 0 メou 1.soek 1. SOClz