1. Provide the products for the following reactions (1 points). NaOH, Ethanol н 2. Draw the...
1. Provide the products for the following reactions (1 points). NaOH, Ethanol 2. Draw the mechanism for the reaction above (2 points). 3. Draw the 1H-NMR for the structure below. Label each peak on the NMR (2 points): DE H CE
1. Provide the products for the following reactions (2 points, 1 point per question). 1) NaOH, Br2 2) H30+ pentanol, H2O+ 2. Draw the mechanism for the following (1.5 point). ethanol, H30+ ОН 3. If you were doing the reaction shown in #2 in lab, how would you use IR to determine if you formed the product or a mixture of product and starting material (0.5 points)? 4. Draw the 'H-NMR for the structure below. Label each peak on the...
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figured this worksheet out and i dont need assistance.
thanks.
1. Provide the products for the following. Assume that the Aldol Condensation occurs (1 points). NaOH, Ethanol 2 2. Draw the mechanism for the reaction above (2 points). 3. Draw the 1H-NMR for the structure below. Label each peak on the NMR (2 points): Hi D
1. Provide the products for the following reactions (3 points, 1 point per question). You will lose credit if you put the group in the wrong position (pay attention to your directing groups). Bry. Felle Rr.FeBry B ellra 2. Draw the 'H-NMR for the structure below. Label each peak on the NMR (2 points):
Predict the products for the following reactions.
Hic NaOH ? HSC ethanol NaOH --> ethanol ? H 1. Br2, PBr3 ? OH 2. H2O Br NaOH --> Cl2 ? H 5. is the reaction of a carboxylic acid derivative with ammonia or an amine to create an amide. a. Hydrolysis b. Alcoholysis C. Aminolysis d. Reduction e. Grignard's reaction 11. Give a mechanism for Fischer esterification utilizing any appropriate starting material you choose.
Please help with both if possible!
1. Provide the missing reactants or products for the reactions shown below. Provide the structure(s) in the boxes provided. (8 points) a. Na o= 1. CH3Mgi 2. H30 2. H:0* 1. CH3Li 2. H30* 2. Provide the reaction mechanism for the reaction shown below. (4 points) cat. H ОН + H2O ОН
2. Give the products for the following aldol reactions. (5 points each) 1. Д. ОН: Н 2. н* 3. ОН: Н ОН ".. 5. ОН + CHO 6. ОН 3. Complete the following scheme. Two step reactions will contain two boxes. 5 points MgBr H CI 5 points AICI: 2. H 3. PCC, CH2Cl2 2 points 5 points 2 points 2. H 3. H Cr04 2 points 5 points OH 2 points 1. OH 5 points Final product shows strong...
predict the IR spectrum and HNMR of 2-bromocyclohexanone
peaks in the NMR spectrum and record the chemical shift, the splitting, an peak in the NMR table below. 1H NMR Data Peak Chemical Shift (6) Multiplicity н Peak Structure: 1 1 5 Br 6 N 3 7 4 8 + Specify the number of hydrogens associated with each peak. 11. Draw the major organic product for each of the following reactions. a. o
Draw a stepwise detailed mechanism and the products(s) for the following reactions: Н-Br 1. CN 2. Н,о CH,ОН Н,о*
provide the reaction conditions and the structure of the
correct products of the following reactions:
0.5 pts Question 2 (10 points) Provide the reaction conditions and the structure of the correct products of the following reactions: B RXN02B н®, сн,он heat А @ heat -H2O С NH The reaction code in the box is: RXN02B RXNO2A RXNO2C CE o