Identify the functional groups that form in each of the
following reactions:
5. Identify the functional groups that form in each of the following reactions: a) addition of a Grignard reagent to a nitrile b) addition of LAH to an amide c) addition of (CH3)2Culi to an acid chloride d) addition of CH2N2 to a carboxylic acid
Question 3.53 a. alkene b. alkyne c. arene d. halide e. alcohol f. ester g. ether h. amine i. amide j. nitrile k. carboxylic acid l. thiol HN Cimetidine (Tagamet) From the list provided, identify the functional groups in this molecule. Enter your answer as an alphabetical series with no commas or spaces Groups present:
Lumili alle for the following compound? - (CH)CHCH.COCH,CH, a. 2-methyl-4-hexanone c. 2-methyl-3-hexanone b. 5-methyl-3-hexanone d. ethyl isopropyl ketonel. 25-Identify the directing effect of the ring substituent in the following reaction: BO, HBO. (a) o.p., activating (b) m-, deactivating (c) o.p., deactivating (d) None of these 26--Ketones are easily reduced to CH3-C-CH3 a-Secondary alcohol b- Primary alcohol c- to acetaldehyde d- to carboxylic acid 27-. What is the structure of the azo group? a-N- b-N-N- C-NEN- d-NEN- 28-What class of organic...
A). 1-Heptene; B). 1-Propene ; C). 1-Butene ; D). CEN E). CH3NH2 ; F). -CO-H; G). CHỊCH,Br; H). NO, nyu, im Krui, ir CH3 OH Настен M H3C MC ;N HỌC-CH-CH, 0). an in the file can os centras 2005,8,0, Consider PHYSICAL PROPERTIES and the E/Z priority of the compounds/substituents above 1. Arrange in ascending order the boiling point and identify the non-covalent bonding : a)compound compounds Q, R, T, U; b) compound B, M, N c),arrange in ascending order...
please answer all these questions, thank you.
CHEM 242L Exp. 4 Report/ Synthesis of Oil of Wintergreen Name Score: 20 1) Assess the effectiveness of the experiment and your technique by A) reporting the yield of each step in grams and percent as well as the overall percent yield (What is "overall percent yield?). SHOW ALL CALCULATIONS! B) Give a complete analysis of the identity and purity of your final product and any isolated intermediates 2 What was the purpose...
N(CH3)3 OH 1. heat 95% 5% (E & Z) он 2. H2N a - Proton transfer dSN2 Nucleophilic substitution b- Lewis acid/base e-Electrophilic aromatic substitution c=E2 elimination f= g Nucleophilic subs at carbonyl(acyl Xfer) h-Conjugate (nucleophilic) addn r-carbonyl nucleophilic addn Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a i for your answers. 1. 2.
N(CH3)3 OH 1. heat 95% 5% (E & Z) он 2. H2N a -...