Draw the major product of the Claisen condensation reaction between two molecules of this ester. Ignore inorganic byproducts. 1. NaOCH3/CH3OH 2. Acidic workup
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- < Question 28 of 85 Submit 1. LiN¹-Pr₂/THF 2. CH3CH2Br CH3 A) This reaction would require a different solvent. B) The base is too weak to deprotonate this compound. C) There is a problem with the order of addition. D) The wrong nucleophilic position was used. Tap here or pull up for additional resourcesProvide an appropriate alkyne starting material A and intermediate product B. Omit byproducts. The number of carbon atoms in the starting material should be the same as in the final product.Draw the major product of the Claisen condensation reaction between two molecules of this ester. Ignore inorganic byproducts. O. 1. NaOCH3/CH,OH 2. Acidic workup Select to Draw
- Write the structural formula of the organic product for the given reaction between an alkyne and an alkyl halide. The alkyne group is shown and should be entered as "CC" without the triple bond. Enter CC before associated HH atoms (e.g., CH3CH2CH2OCHCHCH3). what is the name of the product. 1.NaNH2 CH3CH2CCH------> product 2. CH3CH2Br1. Draw the sulfur‑containing product of the oxidation reaction between two 2‑methyl‑1‑propanethiol molecules. Include all hydrogen atoms. 2. Modify the structure to draw the organic product of the following reaction. Note that [O] is present in excess. Modify the structure to represent the product.When toluene is treated with sulfuric and nitric acids under special conditions, three nitro (NO2) groups are substituted for hydrogens at the 2, 4 and 6 positions on the ring (the next section discusses why the 2, 4, and 6 positions are substituted). The product is a highly explosive substance called 2,4,6-trinitrotoluene. This subastance is commonly known by a three letter name. What is it?
- Bn Draw the structure of the major organic product formed from the reaction below. Bn H ད ་ + HỌỌC. NH2 N DCC .... NH H BnThe conversion of alcohols into alkyl halides by reaction with hydrogen halides is an example of a Nucleophilic Substitution Reaction. This kind of reaction can proceed by two different mechanisms depending on the structure of alcohol substrates used. Generally, primary alcohols are substituted via SN2 mechanism, while secondary and tertiary alcohols undergo SN1 mechanism. Consider the following reaction given in the picture below and the questions in the picture too.Answer all three parts plz. You are starting with three aryl bromides. They undergo a typical grignard reaction with magnesium metal and anhydrous ether (diethyl ether). Dry ice is then added to it and it is then cooled. Draw and label the names of the aryl carboxylic acids that will form for each. Part a) bromobenzene Part b) para-bromoanisole Part c) meta-bromoanisole
- What major alkene product is produced by dehydrating the following alcohols?a. Cyclohexanolb. 1-Methylcyclohexanolc. 2-Methylcyclohexanold. 2,2-Dimethylcyclohexanole. 1,2-Cyclohexanediol (Hint: Consider keto–enol tautomerism.)Draw the major product of the Claisen condensation reaction between two molecules of this ester. Ignore inorganic byproducts. | 1. NaOCH3/CH3OH 2. Acidic workup O Drawing 6When 3-pentanone and ethanol are reacted in an acetal formation reaction in the presence of acid catalyst, the resulting FINAL acetal product has the four different sides of the central carbon. [NOTE: The numbers in the responses bonded to should be subscripted.] [Exam question & (if applicable) response options © 2021 James Y. Chen. All rights reserved.] -СH2CH3, -СН2СНЗ, -ОСН2СНЗ, and -OCH2CНЗ -СH2CH3, -СН2СHЗ, -ОСН2СНЗ, and -OH -Н, -СН2СH3, -ОСН2CH3, and -ОCH2CH3 -(CH2)4CH3, -(CH2)4CH3, -OCH2CH3, and -OCH2CH3 -СН2CH3, -СН2СНЗ, -ОСН2СH2CH3, and -OСН2СH2CH3