Draw the products that result
from each step in the synthesis of
m-bromoaniline.
Draw the products that result from each step in the synthesis of m-bromoaniline. 05 Question (3...
Draw the products that result from each step of the following synthesis. You do not need to include stereochemistry. Draw the products that result from each step of the following synthesis. You do not need to include stereochemistry. 1. EtMgBr 2. H30+ H2SO4, Δ Step 1 Step 2 Step 3
17 Question (2 points) Draw the products that result from the following mechanism, and identify the elementary step. Remember to include all nonzero formal charges and lone pairs. 4th attempt Part 1 (1 pt) Jul See Periodic Table See Hint Draw the products that result from the following mechanism. Remember to include all nonzero formal charges and lone pairs. 120
20 Question (3 points) Predict the products for each step, paying close attention to regiochemistry, where appropriate. If a step can produce more than one product,draw al possible products.Be sure to include all nonzero formal charges. Reagents for step 1: CHCOC, AICI3 Reagents for step 2: HNO, H2SO4 Reagents for step 3: Br2 FeBrs 1st attempt hli See Periodic Table See Hint Step 1 Step 2 Step 3 0 0
13 Question (1 point) Predict the products for each step, paying close attention to regiochemistry,where appropriate. If a step can produce more than one product, draw all possible products. Be sure to include all nonzero formal charges Reagents for step 1:CH COCL AIC Reagents for step 2: HNO3, HSO Reagents for step 3: Bra, FeBr 8th attempt l See Periodic Table See Hint Step 1 Step 2 Step 3
Draw the products that result from each step of the following synthesis. Be sure to include all lone pairs and nonzero formal charges. You do not need to include stereochemistry 2 1)CO2(9) 2) H30* step 2 Br _2Li(s) step 1 Draw ethyl 5-(1-methylethyl)nonanoate.
What is the structure of the last box? Below is a three-step synthesis. Provide the missing organic products for each step. Do not add inorganic side-products or minor products. CH3 1. BH3 THF HBr NaOtBu, HOtBu 6th attempt Feedback i See Periodic Table See Hint 9% 0% HBr NaOtBu BH3/H202 он
The experiment was a multi-step synthesis of p-bromoaniline . Aniline was protected with acetic anhydride . Please help answer the 4 questions posted in the first picture . help of your TA. Questions to be discussed in the discussion section (please see your rubrics next page) 1. Explain why we did not synthesize the target molecule p-bromoaniline by direct bromination of aniline. (1 pt) 2. Explain why we did not synthesize acetanilide by refluxing a mixture of aniline and acetic...
18 Question (3 points) Predict the products for each step, paying close attention to possible products. Be sure to include all nonzero formal charges Reagents for step 1:CHsCOCI, AICI Reagents for step 2: HNOs H2SO4 Reagents for step 3: Br2, FeBr 1st attempt d See Periodic Table SeeHint Step 1 Step 2 Step 3 18/29 8 OF 29 SUBMIT ANSWER
18 Question (3 points) Draw the three requested missing structures for this acetoacetic ester synthesis. Just draw the main organic product of each step-leave out any byproducts 1. NaOEt, EtOH 2. PhCH2Br 3. NaOEt, EtOH 4. CHal 5. NaOH, H2O 6. H30", heat 1st attempt Part 1 (1 point) al See Periodic Table See Hint Draw the product after Step 2:
18 Question (2 points) Draw the major 1.2 and 14-addition products that form as a result of the following reaction between one equivalent each of 2.4-hexadiene and HBr. HBr 1st attempt See Periodic Table O See Hint Part 1 (1 point) Draw the major 1.2-addition product here: