5. Identify the products of the following reactions. You do not need to show the mechanism;...
5. Give the products of the following reactions. You DO NOT need to show a detailed mechanism but do show ALL reaction intermediates. (30 pts) LiAIH4 G CH3-C-00HE (b) F (c) OH CH3 6. Give the product of the following reactions and in each case give a detailed reaction mechanism by which it is formed. (40 pts, 10 each) pH 4-5 ca. H2S4 HBrJ (c)--/SH NaOH I (d) H CH3 H CH3 5. Give the products of the following reactions....
Thank you so much! (2 pts) Draw the major elimination products and Identify the mechanism responsible (E1 or E2). If both E and Z isomers form, only draw the E alkene. If only one isomer forms, label the alkene "E,""Z," or neither 1. NaOCH3 а. Br НОСHЗ b. НОСНЗ C. CI NaOCH3 d. (6 pts) Draw the substitution and/or elimination product(s) for the following reactions and identify 2. the mechanism responsible (SN1, SN2, E1, or E2) for each product drawn....
4.2 Give a detailed mechanism and show the products of the following reactions: OF CH3 C (6] a) C-H E2 ООCH H CHз H b) H3CC E1 CH3 Н-О Br 4.3 Label the following reactions as SN1, SN2, E1, or E2. . Br NaNH2 THE a) HN CI КОН Ethanol b) но Ethanol c) NaOH Ethanol P OH 4A samnle with a.concentration of 0 3 a/ml was nlaced in a cell with a lenath of 5 cm 41
5. Predict the major organic products of the following reactions. Show all asymmetric carbons with wedgeldash notation (i.e., as shown in the starting material). If a reaction produces a racemic mixture, show only one of the enantiomers produced. Carefully note the requested reaction mechanism for each reaction. (20 pts) NaOCH3 CH3OH SN2 Br CH3OH SN1 Br NaOCH3 CH3OH E2 Show Zaitsev product Br CH3OH Br E1
Hello! Just double checking the answers my organic chemistry study guide. Please go ahead and answer ALL the questions you see below, if you can't answer all then PLEASE let someone else do them! High rating only given to ALL questions complete Predict the product(s) for each of the E2 elimination reactions below. Identify the major product for each, 4. Br Heat Cl NaOCH3 Heat Ph кон Page I of 6 5. Show the complete electron pushing mechanism for the...
Help sos 1. Show the expected product(s) of the following reactions. For products containin or cis/trar asymmetric carbon atoms, indicate relative stereochemistry (syn/anti relationships) and/or whether a racemic mixture is produced. (8 pts each) 1. HNO3, H2so4 NO 2. Fe, HCI OCH3 3. NaNO2 aq. HCI 4, CuCN, Δ сно но 1. Br2 H20 2. Fe SO)S b. HO- -H OH s CH2OH 1. SOCI2 2. NH3 H3C 3. Br2 NaOH, H2O 1. KOH 2. PhCH2CH Br 3. NH2NH2 d....
4. Predict the products of the following reactions & indicate whether they are most likely to go through an SN2, SN1, E1, or E2 mechanism. NaCN DMSO NaOH CH3OH heat Only one product is formed in the following E2 elimination reaction. Draw an arrow-pushing mechanism for the reaction and provide the correct product structure. Include a 3-D drawing (chair conformation) displaying proper stereochemistry of the transition state to explain formation of only the major product. CH3 •Br NaOCH3 ~"'CHS
26. Give the arrows (and the required intermediates) to show the mechanism of the following reactions. (3 pts each) Br HBr + a. но. NaH Br b.
6. Identify the most likely mechanism and identify the products aromatic substitution reactions. of the following nueleophilic Ci 1) NaOH, 350°C 2) HCl, H20 1) NaNH2 1) NaOH, 350 °C 2) HCI, H20 ︿Br Cl O2N 6. Identify the most likely mechanism and identify the products aromatic substitution reactions. of the following nueleophilic Ci 1) NaOH, 350°C 2) HCl, H20 1) NaNH2 1) NaOH, 350 °C 2) HCI, H20 ︿Br Cl O2N
4. [12 pts] Propose mechanisms for the formation of all 3 products shown in the reaction below: (draw curved arrows, intermediates, and resonance structures if necessary. NO NEED FOR TRANSITION STATES! CH CH CH CH Br Heat CH,CH,OH OCH.CH Mechanism.14 points) Mechanism 2 points) Mechanism.3 14 points) 5. [14 pts] Provide the major products of reacting the alkene shown in the middle of the scheme below with all the reagents independently. Draw the products' structures in the corresponding table below...