Could you please explain how do I do these type of questions in general? I have no idea what goes in or out of the reaction and why. Would be nice if you could go in detail to even the most basic things, thank you!
Could you please explain how do I do these type of questions in general? I have...
Please explain why only II will proceed. I am having difficulties understanding these questions, thank you! A16 Which of the following reactions would proceed as written? O - T 1. LiAIH4 2. HCI, H20 Me H MeoH Et 1. EtMgBr Me H 2. HCI, H Me OH 1. EtMgBr 2. HCI, H20 Et Me Me OH Me H MeH 1. NaBH4 2. HCI, H,Ó Me OH Tand II. A) B) C) D) E) Tand III. only. Ill only. IV only.
can you please show how eaxh reagent affects the starting material to get to the product 1. EtMgBr, Et20 2. HBO NH a) NaOH b) 1-bromopropane c) HCI, H2O, A d) NaOH, H20 H₂N ONa ONa 1. DIBAL-H, -78 °C ОMe Et 2. MeOH, HCI Оме
As it says in question 2 could you please help me make a flow chart like the provided example below? 2) For the portion of the procedure shown below, create a flow chart for the acid-base extraction at the end of the Grignard Reaction in a similar manner to the one on Canvas for the extraction lab. Start your flow chart with the crude reaction mixture before addition of HCl and continue it until the product is recovered. Depict the...
hi, if i could please have help with this question. will rate asap:) thank you 1. (10 points) Predict the major organic product or products for each of the following. Be sure to include stereochemistry where appropriate. Assume each is in the most appropriate solvent. Remember, "no reaction" may be an answer. H, H20 b) H* HCI HO a) BH3 b) HOO
no explanation needed, I just need the right answer choices. Thank you!! Predict the major organic product of the following reactions. Assume one equivalent of reagent unless otherwise stated, it's a solvent, oxidizing, or reducing agent. If no reaction will occur, choose E. Be mindful of stereochemistry. Me Me 1. Mgº, THE o Br Me H Me 1 Me 3. H20, HCI Me Y Me Me Me Me Me Me Me HO он Me Me Me Me Predict the major...
please help me solve questions 16,17,18,19 and 20. thank you. THE FOLLOWING SCHEME APPLIES TO QUESTIONS 16, 17, 18, 19 AND 20 ce OH . 121 QUESTION 16 The reagent required for step (O is A B SOC. HCI NaCl in water 12] QUESTION 17 Which of the following reagents can be used to achieve step? А CO, in acid or periodinane LAH, in ether, or Nath. in ethanol KMnO, in acid MCPBA in CHO C 121 QUESTION 18 The...
You do not have to consider stereochemistry. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate multiple products using the + sign from the drop-down menu. Draw the structure of the major organic product(s) of the reaction. 1.2 MgBr, ether yuda en 2008, cover CI 2. H20* CH3 Draw the structure of the major organic product(s) of the reaction. Culi ether, -78° C H3C Draw the structure of the major organic...
can you please explain to me what i am supposed to do here? i do not understand. et + 3 Bra OOH + Soch I CH₃ CH₂ CH₂ SH + NaOH 7. (18 points) Write the organic products for the following reactions: 2. CH₃CHCH₂CH H+ heat CH3
i need help with post questions, thanks Product Isolation After stirring the reaction for 5 minutes and allowing the reaction mixture to cool (the reaction can be exothermic), remove the Claisen head from the conical vial. Slowly add 3 M HCl(aq) drop-wise. The solid may need to be broken up with a stirring rod or a pipet. Continue to add acid until the aqueous phase (bottom layer) tests positive with pH paper. Extractions can be done using the conical funnel...
Could someone please explain how to do this. Thank you. If you could explain in detail so I could understand I would appreciate it very much! Provide curved arrows to indicate the mechanism involved in each step of the following Hantzsch pyridine synthesis. 0 OH OH OH 0 он о O HO NH3 OH O H2N он он OH H