a carboxylic acid can be synthesized by?
Homework Answers
1. Only first option is correct, chromium trioxide with sulphuric acid forms a catalyst known as jones reagent and it is useful for oxidation of primary alcohol and aldehydes to carboxylic acids and secodary alcohol to ketones.
2. primary alcohol with PCC(Pyridinium chlorochromate) oxidized to aldehydes, but when used with DMF it furthere oxidize the compound to carboxylic acid.
3. Cleavage of alkene with ozone in presence of DSM(dimethyl sulphide) produces carbonyl compounds.
4. Reduction of ester with DIBAL yields the aldehydes.
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a carboxylic acid can be synthesized by?
Question 14 1 pts A carboxylic acid can be...
Identification of which of the following types of reactions serotonin can experience
The molecule is serotonin. (C₁₀H₁₂N₂O.)1) Identify which of your functional groups goes with which reaction • Hydrogenation (alkenes and alkynes) • Hydration (alkenes and alkynes) • Oxidation (primary/secondary alcohols, aldehydes, and thiols) • Reduction (aldehydes and carboxylic acids) • Neutralization (carboxylic acids and amines) • Esterification (alcohols and carboxylic acids) • Amidation (primary/secondary amines and carboxylic acids) • Hydrolysis (esters and amides)2) Identification of what new functional groups will result from what you identified from these organic reactions.
Can you give me a few examples of these type of reactions? Thanks Synthesis of RCO_2H...
Can you give me a few examples of these type of reactions?
Thanks
Synthesis of RCO_2H Oxidative cleavage of mono- or 1, 2-disubstituted alkenes, using KMnO_4 HO-, H_2O, heat Oxidation of 1 degree alcohols or aldehydes, using KMnO_4 or aqueous H_2CrO_4, and Ag_2O or Ag(NH_3)_2OH Oxidation of alkyl benzenes with KMn04, HO*, H20, heat, to form benzoic acids
1. What is the key feature about the Jones oxidation of primary alcohols to carboxylic dar...
1. What is the key feature about the Jones oxidation of primary alcohols to carboxylic dar aw't PCC or PDC do this? A partial mechanism will aid in your explanations. 2. Compare and contrast the following reduction reactions. Again, mechanisms can aid your explanations. LiAIH4. THF NaBH4 then H20, HCI CH3OH
Need help with questions 2-4. Information: Just as it is beneficial to make a summary of...
Need help with questions 2-4.
Information: Just as it is beneficial to make a summary of the types of reactions, it is a list of the functional groups that commonly react by each of the Seven summary is shown in Table 2. is also useful to the ven pathways. Such reaction pathways Table 2: Functional groups that commonly react by the seven react acid-base - carboxylic acids, phenols (acids) - amines (bases) addition - alkenes, alkynes elimination - alcohols reduction...
Cleaving Alkenes with Ozone (0) - treatment of alkenes with ozone followed by mild reduction leads...
Cleaving Alkenes with Ozone (0) - treatment of alkenes with ozone followed by mild reduction leads to the formation of ketones and aldehydes y 0, CHC-78 - Zn/H30 Zn/4309 malozonide ozonide 1.0, CH,Ch, -78° 2. Zn/H30* 1.O, CHÚC-78°. 2. Zn/H30* Cleaving Alkenes with Potassium Permanganate (KMnO4) - treatment of alkenes with KMnOin acidic solution leads to the formation of ketones and carboxylic acids: KMnO4, H,0* KMnO, H,O* KMnO4 H2O* Epoxidation of Alkenes-treatment of alkenes with peroxy acids leads to the...
14) Which of the following reagents would react with a primary alcohol to produce an aldehyde as the final product?...
14) Which of the following reagents would react with a primary alcohol to produce an aldehyde as the final product? A) PCC B) H2SO4 C) H2Cr04 D) CH3MgBr, followed by HCI - 15) Which one of the following is not oxidized by K2Cr2O7 in H2SO4/H20? A) isobutyl alcohol B) tert-butyl alcohol C) sec-butyl alcohol D) n-butyl alcohol 16) Which of the following methods will NOT produce an alcohol as the product? A) hydroboration-oxidation of an alkene B) oxidation of an...
14) Which of the following reagents would react with a primary alcohol to produce an aldehyde as the final product?...
14) Which of the following reagents would react with a primary alcohol to produce an aldehyde as the final product? A) PCC B) H2SO4 C) H2C704 D) CH3MgBr, followed by HCI 15) - 15) Which one of the following is not oxidized by K2Cr2O7 in H2SO4/H20? A) isobutyl alcohol B) tert-butyl alcohol C) seo-butyl alcohol D) n-butyl alcohol 16) 16) Which of the following methods will NOT produce an alcohol as the product? A) hydroboration-oxidation of an alkene B) oxidation...
True and False questions!! 1. True and False Question (1) Carbonyl compounds have higher boiling points...
True and False questions!!
1. True and False Question (1) Carbonyl compounds have higher boiling points than hydrocarbons, but lower boiling points than corresponding alcohols. (2) Aldehydes and ketones react with primary amines to form imines and with secondary amines to form enamines. (3) Aldehydes and ketones can be oxidized to carboxylic acids. (4) Diols can form acetal with the ketone or aldehyde to protect them for selective reduction of the ester (5) The electron-withdrawing group in Wittig reagent does...
1. True and False Question (0.5 point per question) a) Carbonyl compounds have higher boiling points...
1. True and False Question (0.5 point per question) a) Carbonyl compounds have higher boiling points than hydrocarbons, but lower boiling points than corresponding alcohols. b) Aldehydes and ketones react with primary amines to form imines and with secondary amines to form enamines. c) Aldehydes and ketones can be oxidized to carboxylic acids. d) Diols can form acetal with the ketone or aldehyde to protect them for selective reduction of the ester. e) The electron-withdrawing group in Wittig reagent does...
I would like all of them answered first 4 are True 1. True and False Question...
I would like all of them answered
first 4 are True
1. True and False Question (1) Carbonyl compounds have higher boiling points than hydrocarbons, but lower boiling points than corresponding alcohols. (2) Aldehydes and ketones react with primary amines to form imines and with secondary amines to form enamines. (3) Aldehydes and ketones can be oxidized to carboxylic acids. (4) Diols can form acetal with the ketone or aldehyde to protect them for selective reduction of the ester (5)...
Can you give me a few examples of these type of reactions?
Thanks
Synthesis of RCO_2H Oxidative cleavage of mono- or 1, 2-disubstituted alkenes, using KMnO_4 HO-, H_2O, heat Oxidation of 1 degree alcohols or aldehydes, using KMnO_4 or aqueous H_2CrO_4, and Ag_2O or Ag(NH_3)_2OH Oxidation of alkyl benzenes with KMn04, HO*, H20, heat, to form benzoic acids
1. What is the key feature about the Jones oxidation of primary alcohols to carboxylic dar aw't PCC or PDC do this? A partial mechanism will aid in your explanations. 2. Compare and contrast the following reduction reactions. Again, mechanisms can aid your explanations. LiAIH4. THF NaBH4 then H20, HCI CH3OH
Need help with questions 2-4.
Information: Just as it is beneficial to make a summary of the types of reactions, it is a list of the functional groups that commonly react by each of the Seven summary is shown in Table 2. is also useful to the ven pathways. Such reaction pathways Table 2: Functional groups that commonly react by the seven react acid-base - carboxylic acids, phenols (acids) - amines (bases) addition - alkenes, alkynes elimination - alcohols reduction...
Cleaving Alkenes with Ozone (0) - treatment of alkenes with ozone followed by mild reduction leads to the formation of ketones and aldehydes y 0, CHC-78 - Zn/H30 Zn/4309 malozonide ozonide 1.0, CH,Ch, -78° 2. Zn/H30* 1.O, CHÚC-78°. 2. Zn/H30* Cleaving Alkenes with Potassium Permanganate (KMnO4) - treatment of alkenes with KMnOin acidic solution leads to the formation of ketones and carboxylic acids: KMnO4, H,0* KMnO, H,O* KMnO4 H2O* Epoxidation of Alkenes-treatment of alkenes with peroxy acids leads to the...
14) Which of the following reagents would react with a primary alcohol to produce an aldehyde as the final product? A) PCC B) H2SO4 C) H2Cr04 D) CH3MgBr, followed by HCI - 15) Which one of the following is not oxidized by K2Cr2O7 in H2SO4/H20? A) isobutyl alcohol B) tert-butyl alcohol C) sec-butyl alcohol D) n-butyl alcohol 16) Which of the following methods will NOT produce an alcohol as the product? A) hydroboration-oxidation of an alkene B) oxidation of an...
14) Which of the following reagents would react with a primary alcohol to produce an aldehyde as the final product? A) PCC B) H2SO4 C) H2C704 D) CH3MgBr, followed by HCI 15) - 15) Which one of the following is not oxidized by K2Cr2O7 in H2SO4/H20? A) isobutyl alcohol B) tert-butyl alcohol C) seo-butyl alcohol D) n-butyl alcohol 16) 16) Which of the following methods will NOT produce an alcohol as the product? A) hydroboration-oxidation of an alkene B) oxidation...
True and False questions!!
1. True and False Question (1) Carbonyl compounds have higher boiling points than hydrocarbons, but lower boiling points than corresponding alcohols. (2) Aldehydes and ketones react with primary amines to form imines and with secondary amines to form enamines. (3) Aldehydes and ketones can be oxidized to carboxylic acids. (4) Diols can form acetal with the ketone or aldehyde to protect them for selective reduction of the ester (5) The electron-withdrawing group in Wittig reagent does...
I would like all of them answered
first 4 are True
1. True and False Question (1) Carbonyl compounds have higher boiling points than hydrocarbons, but lower boiling points than corresponding alcohols. (2) Aldehydes and ketones react with primary amines to form imines and with secondary amines to form enamines. (3) Aldehydes and ketones can be oxidized to carboxylic acids. (4) Diols can form acetal with the ketone or aldehyde to protect them for selective reduction of the ester (5)...
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