Q: What is reductive amination explain with example?
A: The solution is given below -
Q: Discuss order of reactivity of following with reason: Acid Halide, Acid Anhydride, Esters, Acid…
A: In case of acid derivatives, the carbonyl carbon (which has partial positive charge on it) is…
Q: what causes an alkane, alkene, and alkyne differ in acidity Please explain. I understand that the…
A: Alkyne is sp- hybridized. Alkene is sp2 hybridized. Alkane is sp3 hybridized. More the S character…
Q: Why are 2-nitrobenzoic acid and 2-chlorobenzoic acid stronger acids than benzoic acid?
A:
Q: Pyridine (left) and pyrrole (right) are both nitrogen-containing aromatic heterocycles. They look…
A:
Q: In the presence of excess base and excess halogen, a methyl ketone is converted to a carboxylate…
A: Methyl ketone is a kind of ketone in which methyl group is attached to the carbonyl group. This…
Q: Provide the IUPAC names for the following compounds. (a) (b) (c)
A: Systematic Name: It is a standardized name given for a chemical compound in systematic manner. Any…
Q: Give a clear handwritten answer with explanation. ..give below some options choose the in which…
A: Tollen''s reagent is the reagent used in chemistry. It consists of a solution of silver nitrate,…
Q: Rank imidazole, pyrrole, and benzene from most reactive to least reactive toward electrophilic…
A: Electrophilic substitution reaction- The replacement one atom or group of atom from reactant species…
Q: Draw the organic product of the following hydrogen and include all hydrogen atoms.
A: Alkynes on hydrogenation reduces to alkenes. The triple bond in the alkyne is weak and reduces to…
Q: In the presence of excess base and excess halogen, a methyl ketone is converted to a carboxylate…
A: In halo from the reaction, A methyl ketone gets converted into carboxylate ion, and the leaving…
Q: Predict/draw the neutral organic product of the reaction.
A: Step 1 → Formation of carbo cation forming Markovnikov's rule
Q: Show how methyl amine, shown below, can hydrogen bond to other methyl amines by clearly drawing in…
A: Hydrogen bonding can take place between a highly electronegative atom and hydrogen. Intramolecular…
Q: Result obtained in the reaction between acetylene and ammoniacal silver chloride
A: Acetylene is the simplest and first Molecule of alkyne family, with Molecular formula of C2H2 , its…
Q: How to determine the relative basicity of nitrogen heterocycles ?
A: Heterocyclic compounds are aromatic hydrocarbons with one or two hetero atoms like O or N. Some well…
Q: Only two of the following carbonyl-containing compounds have a large equilibrium onstant for…
A:
Q: How the synthesis is conceptually divided ?
A: A sound knowledge of mechanistic organic chemistry, detailed information on the art and science of…
Q: Compare the basicity of piperidine and pyridine ?
A: Piperidine is the six membered ring in which one member is nitrogen. Pyridine is also a six membered…
Q: Why would oxygen of carbonyl be protonated but not amide nitrogen in this reaction?
A:
Q: Step by step Procedure for Test of Aldehyde with a Conclusion
A: Organic compounds can be defined as the compounds that contain carbon and hydrogen atoms in a…
Q: The byproduct of the photo dimerization of benzophenone to benzopinacol is?
A:
Q: Why are the cyanates and sulfonates not as toxic as the other compounds of cyanide?
A: Cyanide is the CN-particle, and as a harm it is generally controlled as one of the three mixtures…
Q: How many different products obtained upon ozonolysis of are ?compound A
A: unsaturated compounds (alkynes,alkenes etc) reacts with ozone to form carbonyl compounds ,.…
Q: Explain and show how did the lettered compounds found in each reaction in letter a and b only. this…
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Q: With the Aid of relevant equation describe four methods that can be used to prepare carbonyl…
A: Carbonyl compound are compound which have C=O functional group They are nothing but aldehyde and…
Q: Give introduction about Acid/Base Extraction.
A: Аn асid-bаse extrасtiоn is a mean оf liquid-liquid extrасtiоn. It generally invоlves…
Q: The amide substituent effects. the acidty of phenol by the negative charge of the phenoxide through
A: Let us discuss the acidity of phenols and effects of substituents.
Q: explain in detail how you would separate benozic acid from phenol, using either lithium hydroxide,…
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Q: Arrange the following in terms of decreasing acidity. Type the letter labels for each structure on…
A: Acidic strength of organic acids like carboxylic acids, alcohols and phenols depends upon its…
Q: 1. What is the definition of acidity? 2. Compare the acidity of ammonia and its aliphatic…
A: Acidity means ability to donate a proton
Q: Weak base can react with strong acid to form salt. Will pyridinium salt be more aromatic than…
A: Interpretation- To explain pyridinium salt be more aromatic than pyridine and to explain it with…
Q: Aside from H₃O⁺, the other product during the dissociation reaction of HN₃ is _____ and it is the…
A: In this question, we will selected the correct answer for the dissociation reaction of HN3 in water.…
Q: CH₂OH H
A: Here we have explain major product formed in the following given reaction.
Q: How would you explain why phenol is the o-p director, while nitro benzene is m-directional?…
A:
Q: the reduction of α-methylvaleraldehyde, results to?
A: Reduction of aldehyde give alcohol
Q: Imidazole is more basic than pyridine, but more acidic than pyrrole, why?
A: A question based on acidic and basic nature, which is to be accomplished.
Q: c) Rank the following compounds in order of increasing reactivity toward nucleophiles. Explain your…
A: There are many mechanisms in organic chemistry such as nucleophilic substitution, nucleophilic…
Q: answer with explanation and give the mechanism with curved arrow given bleow reaction !!
A:
Q: (a) Arrange the following compounds according to their reactivity towards electrophile. Justify your…
A: We must know that more aromatic a compound is, more stable it will be and thus less reactive. A…
Q: Arrange the following in order of decreasing reactivity to nucleophilic addition: ketone, aldehyde.…
A:
Q: Consider the below molecule and its hydrogen atoms labeled a through e. Rank the named hydrogen…
A: acidity - increase order - Hd<Hc<He<Ha<Hb
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Solved in 2 steps
- Give a clear handwritten answer with explanation. ..give below some options choose the in which given options who react with Tollen's reagent...give textual explanation also...?In paragraph/essay form:Provide an explanation (in detail) on how base catalysts speed up nucleophilic reactions of carbonyl compounds.Arrange the following compounds according to their rate of solvolysis with suitable explanation.
- A- What is the definition of acidity? B- Compare the acidity of ammonia and its aliphatic derivatives with of acidity pyrrole C- Melting points of pyrrole is higher than melting point of 1-methyl pyrrole explain your answer D- Why does pyrrole prefer electrophilic substitution reactions? E- Why Pyrrole is considered to be an aromatic compound ? F- Explain the Reimer-Tiemann reaction mechanism of heterocyclic compounds? G- Why pyridine is a weak base? explain your answer? H- Pyridine can react with electrophiles, electrophilic substitution ? explain your answer ? G- Explain the Diels–Alder reaction mechanism of heterocyclic compounds? I- From a-haloketone how can you prepared flowing compounds : Imidazole Oxazole Thiazole J- compared the acidity and basicity of Pyrazole and Imidazole with Pyrrole and Pyridine ?Arrange the following compounds in increasing acidityArrange the following in order of increasing reactivity towards a hydrogen halide and explain.
- Explain the reaction for the formation of acetal and hemiacetal. Explain why N,N-disubstituted amide is less acidic than ester. Why only methyl ketone do undergoes haloform reaction. LDA is the base of choice for carbonyl compound to completely convert into enolate. Why?Describe a sequence of reactions for the following reactionGive a clear handwritten answer with explanation and give the mechanism with curved arrow given bleow reaction !!
- With the use of resonance structures, explain why OH group of phenol is an ortho/para director. Provide illustration as needed.Rank the acidity of each of these compounds from least to most acidic. The explicitly drawn Hydrogens should be compared. What would be a small explanation as to why they are ranked in that order?Rank and explain the following compounds in order of increasing acidity