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please answer and show work for stepwise synthesis and other questions. 1. Provide a stepwise synthesis...
Provide a stepwise synthesis for the following compound using benzyl alcohol as you only source of carbon & using any other reagents necessary OH
7) Provide a stepwise synthesis for the following compound using benzyl alcohol as your only source of carbon and using any other reagents necessary. OH OH benzyl alcohol
Propose a stepwise synthesis for N-propylbutanamide. using 1-proanol and/or carbon dioxide as your only source of carbon and using any other reagents necessary. Detail how the final product could be identified using a spectroscopic method.
72. Predict the product for the following reaction. CH,CH,OH pyridine A) ethyl 3-methylbutanoate B) ethyl 2-methylpropanoate C) isobutyl ethanoate D) 5-methyl-3-hexanone E) none of these 73. Predict the product for the following reaction. 1 soa 2.CH.CH.NL 74. Predict the product for the following reaction. 75. Predict the product for the following reaction sequence. ooo AICI, 76. Provide the reagents necessary to carry out the following conversion.
1. Identify the amino acids in the following tripeptide and provide the major structure of the tripeptide at pH 3, 7, 12. H O ?? ?? 2a. Ideally, one could synthesize a peptide without the use of protecting groups In the following problem, provide a mechanism for the synthesis of the dipeptide Phe-Trp. Assume that the only product formed is Phe-Trp. N-C-N Ph (DCC) OH Phe-Trp
Please answer all components. Question 7 (15 points) Propose a stepwise synthesis for the following reaction. You may use any reagents and/or additional molecules that you wish Question 8 (15 points). Provide a stepwise synthesis for the following reaction. (There are multiple synthesis pathways)
Provide the necessary reagents and conditions for the series of steps necessary to carry out the synthesis of the compound shown, using propyne as the only carbon source. (You can have unlimited amounts of propyne, and any other organic or inorganic reagent, solvent, etc., but you have to make all the carbon compounds you need out of propyne, somehow or another...). Name: . solvent, etc., but you have to make all the carbon compounds you need out of propyne, somehow,...
In class Ch 19 and 20 Provide the reagents necessary to carry out the following conversion. 1. -N OH он Draw the Mechanism КОН H2N-NH2 CN Он Нао
b) Write the structure of the following compounds (Fischer projection): (D)-serine, (S)-methionine c) Write the structure of the following tripeptide: H-Ala-Pro-Phe-OH 2. Determine the N-terminal amino acid of the above tripeptide (H-Ala-Pro-Phe-OH) using the Sanger method (chemical equation). 3. Starting from alanine and glycine synthetize the glycyl-alanine (H-Ala-Gly-OH) dipeptide using mixed anhydride coupling method with Boc (amino) and Bn (carboxyl) protecting groups (reagents, reaction conditions, chemical equations). 4. Starting from the appropriate aldehyde synthetize alanine using the Strecker synthesis (reactions,...
Organic Chem 2: please help! 26) Provide a detailed, stepwise synthesis for preparing the molecule on the left below from the molecule on the right and any other reagents necessary Br он