answer all three questions and circle the answers Which of the following reactions will not produce...
please answer all 4 questions and circle the answers to make
it clarified
H11.11 - Level 2 Homework . Unanswered For the given reaction, predict the major and minor products or not produced if the product is highly unlikely to form. CH.CH OH major and minor products Premise Response Drag and drop to mat H11.12 - Level 2 Homework. Unanswered For the given reaction, predict the major and minor products or not produced if the product is highly unlikely to...
There should be four answers to this question. The answer
choices are as followed: major, minor, or not produced.
H11.12-Level 2 Homework Unanswered For the given reaction, predict the major and minor products or not produced if the product is highly unlikely to form. major and minor CH,CH,ONa H CH,CH,OH products CH, H H 4) 1) 3) Premise Response Drag and drop to match 1 1) = A Major = B Not produced 2 2) 21 Br
H9.7 - Level 1 Homework – Unanswered Identify the major and minor El products formed in the following S1/E1 reaction? Br CH,CH,OH - heat major E1? minor E17 Premise Response Drag and drop to match 1 1) → = A Major → = B Minor ^ . 40 ENG 11/19/2019
There should be seven answers to this question. The only answer
choice i am looking for is it minor or major. Also one out of the
seven answer choices should be not produced.
H11.11 - Level 2 Homework . Unanswered For the given reaction, predict the major and minor products or not produced if the product is highly unlikely to form. CH.CH OH major and minor products Premise Response Drag and drop to mat
21) Which of the following reactions will produce the given product in good yield? Select all that apply он CH3OH a) OSO,CH3 Br NaBr (CH3)3COH b) O=U CH3 Nal c) acetone OSO,CH3 MeoNa Меон OH e) MeONa MeOH
help with all of these !
Question 8: Which is the better retrosynthesis for the given target molecule? Explain and provide a one-step synthesis of the target molecule. Br Br Hас Hас Hас .CH3 b) NaQH CHy Question 7: Draw the plausible mechanism for each of the folllowing transformations: a) CHy Не нс CHs CH СH, CH3 conc. H,SO -CH3 heat CH он Question 5 Predict the major and minor products for the following reactions: a) NaSH Н,с b) Br...
Question : Predict the major and minor products for the following reactions: NASH -CH3 + 1 H30 HC b) NaOEt Question 6: Predict the major and minor products for the following reactions: NaOEt OTS - Tosylate (OTS) With on CHM 2210 CH3 NaOH H₂C O=O=O Question 7: Draw the plausible mechanism for each of the following transformations: CHE BECH HO HBr CH CH CH3 H₂C- conc. H,SO heat HC Insuu H Question 8 Which is the better retrosynthesis for the...
answer all questions
5. Fill in the missing structures (products or reagents, including stereochemistry, if relevant) and specify the most likely mechanism (SN1, S2, E1, E2) for formation of the product you have drawn. If a mixture will occur,show the major products. CH,ONa Сн,он нсулснэ H₃C Br HO H2O/acetone H₃C LIOH CH₂ H₂c a DMF 6. For the series shown below, label the most stable alkene, and the least stable alkene. CHE CH, CHE CH, -CH3
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....
Homework. Answered Which is not true of the Transmission Control Protocol (TCP)? Multiple answers: You can select more than one option O A it supports full duplex communication o B it has graceful connection shutdown O с its connections are logical D it uses the message paradigm E it is an end-to-end protocol O F None of the above Answered Change your responses to resubmit Match the NIST Framework Category with the Task Premise Response Drag and drop to match...