I seem to be having trouble with this reactions step by step. if you could help...
These synthesis reactions are kicking my butt and I'd appreciate some help with how to go about answering these, or if anyone has any pointers on how to look at these types of problems. Thank you! Specify the reagent you would use in each step of the following synthesis: CH3 H3C CH3 step 1 step 2 H3C CH3 Reagents Available a. LiAIHA b. H2SO4 c. HCI f. PBr3 K. CH3CH2MgBr g. Dess-Martin periodinane (DMP) L. CH MgBr (phenylmagnesium bromide) h....
1. Predict the major produc t for the following reactions. (1) CO2 (2) Ho MgBr H,O SOCI CEN dine Cl OH excess NH Ci (CH3)2CuLi Cl (1 excess CH CH2MgBr Ci (2)H20 SOCI NH2 SOCI OH
I need help in Organic Chemistry! I am having trouble with these problems, please help!! I appreciate you! 4. For each of the following sets of material and products propose a synthesis using reactions from Chapters 1-11 of the textbook. Remember to consider stereochemistry where appropriate. Show the product of each step you propose. There are more than one solution for each You do NOT need mechanism, only conditions. a. H-CEC-H
can you show me what each step looks like? im having trouble seeing how the 3 ketones come in. thank you so much 16.28 Predict the major product from each of the following reactions MMOD (a) H (1) MgBr (excess) (2) H2O* (3) H2CRO4 anoioso ALDEHYDES AND KETONES. NUCLEOPHILIC ADDITION TO THE CARBONYL GROUP 387 (1) 16.28 (a) MgBr (excess) н (2) H30* (3) H2CRO4
Specify the reagent you would use in each step of the following synthesis: step 1 step 2 step 2 Reagents Available a. LIAIHA f. PBr3 b. H2SO4 c. HCI d. HBO e. SOC2 k. CH3CH MgBr g. Dess-Martin periodinane (DMP) I. CH.MgBr (phenylmagnesium bromide) h. Nah m. (CH3)2CHMgBr 1. NaOH n. Croz J. CH3MgBr Write the letters of the reagents in the boxes below. Reagent for step 1 Reagent for step 2 Submit Answer Retry Entire Group 9 more group...
Im having trouble with these questions and i cant find a good example in my textbook. Any help would be greatly appreciated! 3) Fill in the boxes with the missing product or reagents needed in the following reactions. Each line is a separate reaction. (3 pts each) SOCIE Pyridine Pyridine HSY Pyridine Pyridine O= Pyridine KCN 1) MgBr 2) H,0 (Acid work up) Email ID 1) Draw the mechanism of the acyl substitution reactions shown below. Proton transfer steps are...
14. (4 points each) Complete the following reactions showing the major organic product). 2 CH,NH CH CH,OH Ci pyridine 2. 2CH,NH2 Ci AICl I. excess CH,MgBr 2. H CH,CH,CH OH NaOH 14. (4 points each) Complete the following reactions showing the major organic product). 2 CH,NH CH CH,OH Ci pyridine 2. 2CH,NH2 Ci AICl I. excess CH,MgBr 2. H CH,CH,CH OH NaOH
Can I get help with 1 and 2? Week 9 Lab Quiz - Grignard Reactions Please answer these questions on a blank piece of paper or on a printout of this page. 1. Draw the products of the following Grignard reactions CH,MgBr. CH3 MgBr CH3MgBr O=O=0 2. Name the circled functional groups on taxol and fentanyl: NH O oo" LE. taxol
References) Specify both the alcohol starting material and the reagents you would use in each step in a synthesis of the compound shown. If the synthesis requires only two stepsenter "none" for step 3. Alcohol Starting Materials 1. methanol 2. ethanol 3. 1-propanol 4.2-propanol 5. cyclohexanol Reagents available f. PBry a. LiAlH b. H2SO4 c. HCI d. HBr e. SOCI, CrO3, H, SO, H,O NAH I. CH, MgBr; then H, O* J.CH,CH, MgBr, then H, O k. CHỊ CHỊCH, MgBr,...
im having trouble with #4 molsolute -I = I solution 3. Calculate the moles and grams of NH OH present in 30.0 mL of a 1.50 M NH OH solution. (See the molarity formula.) O 30.0 L = 10.145 moll IL soln = 1.577 0.045 mol NHg Ott 135.otleg NipH 1 Imolto Hot 4,5810-2 mol - 1.58. 4. Would the 30.0 mL of 1.50 M NH OH from problem 3 be sufficient to react with 4.2 g of CuSO4.5H2O? Show...