Arrange the following compounds in order of decreasing reactivity towards hydrolysis. H2N. H3CO NAI IYK КАН BCS

Q: Rank the following compounds in the order of INCREASING acidity. но но он II II IV

A: Ans) 2<4<3<1

Q: a. H2C=CH2 b. (CHз)2С%3CH2 c. CH3CH=CHCH3

A: Increasing order of reactivity : a < c < b Reactivity of alkene towards hydrohalogenation is…

Q: Rank the attached compounds in order of increasing basicity

A: The basicity of any molecule is proportional to the tendency of molecule to donate electron pair…

Q: Rank the following compounds in order of increasing acidity: COOH ОН CH3 СООН NO2 CI I II III IV

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Q: Rank the following compounds in order of increasing acidity of their most acidic hydrogen atom.…

A: Acidic character of an organic compound depends on the stability of its conjugate base. If an…

Q: Rank the attached compounds in order of increasing acidity.

A: The ability of a compound to donate hydrogen ions is called acidity. The acidic nature or acidity is…

Q: Identify the products obtained by the hydrolysis of the given compound. i i -COC- one molecule of…

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Q: Choose any bases that will selectively deprotonate the above acid, that is, any bases that will…

A: A base can deprotonate any acid only if its pka is greater than the pka value of conjugate base of…

Q: Arrange the following compounds in order of decreasing their acidity (most first) I. H20 II. C2H6…

A: The acidic strength of any compound depends on the stability of their conjugate bases. with the…

Q: Explain why carboxylic acids do not undergo nucleophilic acyl substitution reactions with amines.

A: A chemical species which has high electron density or a lone pair of electrons, by using which it…

Q: Which of the following substituted phenol is the strong acid? I- p-nitrophenol Il-p-methoxyphenol I-…

A: Given question is belong to acidity.

Q: Arrange each group of compounds in order of increasing acidity.(a) phenol, ethanol, acetic acid

A: The pKa values of given compounds are, Acetic acid = 4.8 Phenol = 10 Ethanol = 16 In generally more…

Q: Which of the following is the appropriate reactants for the synthesis of pyrrole derivative below.…

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Q: of NaOH (а) H2O OCH3 (b) NH3 + OCH3 HCI (с) CH3CH2OH + OCH3

A: We have reaction of ester with NaOH , ammonia and ethanol.

Q: Which of the following compounds will form a yellow solid when dissolved in a basic, aqueous…

A: Iodoform test: The Ketones and aldehydes which have a CH3CO group can react with iodine in a basic…

Q: Which of the following will readily undergo decarboxylation upon heating?

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Q: (II) Provide the IUPAC name for the following carbonyl compounds. PHCH2CH(CH3)CH2CH2CHO…

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Q: Which of the following carboxylic acid derivatives is the least reactive towards a nucleophilic…

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Q: What is the problem with running the following reaction? NH2 HNO3 H2SO4 It will result in multiple…

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Q: Draw the main organic product formed in each of the following reactions: (a) (b) (c) O + H₂O OCH3…

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Q: Rank the following in order of increasing basicity. coo coo" coo

A: Rank the following structures according to basicity

Q: Which of the following chemical species is considered as strongly basic nucleophile? а. Cyanide ion…

A: The substances with strongly basic nucleophile has to be given.

Q: Which of the following nucleophilic substitution reactions will take place?

A: Better leaving group is a weak base. The sequence of leaving group from better to worse is I- >…

Q: Rank the attached compounds in order of increasing basicity.

A: Basicity of the aniline depends on the substituents. If electron withdrawing groups  are presesnt…

Q: Rank the following compounds in order of increasing acidity. А: В: С:

A: Applying concept of aromaticity and %s character.

Q: Rank the following compounds in order of increasing acidity

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Q: Which of the following bases most favors elimination over substitution? (CH3)3CO- O H2O CH30- CN-

A: More basic  anion most favors  elimination reaction over substitution.

Q: Rank the compounds in each group in order of increasing basicity.

A: Basicity- The ability of compound to donate lone pairs of electrons or accept protons is called…

Q: Which of the attached nucleophilic substitution reactions will takeplace?

A: Reason for option a: Reaction of cyclohexylamine with I- does not take place because primary and…

Q: Of the following carbonyl compounds, which will contain the lowest percentage of hydrate when mixed…

A: Greater is the reactivity of the carbonyl higher will be the percentage of hydrate.  In case of…

Q: Explain why the reaction in Problem 18.48 proceeds dramatically more slowly under neutral conditions…

A: The given reaction is,

Q: Rank the following compounds in order of increasing basicity: NH₂ NH₂ NH₂ NH₂ A) B) D) OCH3 NO₂ 2

A:

Q: acetaldehyde lactic acid - acetic acid Il only I only I and II I and III I, II, and III

A: Option A is correct choice || Only

Q: Which of the following compounds can serve as Michael acceptors?

A: A compound with α, β-unsaturated carbonyl group can act as Michael acceptor.

Q: Arrange the following in compounds in INCREASING reactivity to hydrolysis. Drag the structures to…

A: The molecules given in the options are acid derivatives with -Cl, -CH2CH3 , and -NH2 groups attached…

Q: Which of the following reactions represents the most likely reaction of naproxen with water? a.)…

A: • Naproxen (C14H14O3) is the  anti-inflammatory agent in Aleve and Naprosyn

Q: Which factors impact the relative stability of the two indicated bases, and in what way? O2N A

A:

Q: Which labeled atom will most likely react when acetic acid is treated with sodium hydroxide? Ο Α

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Q: Carboxylic Acid Derivatives Resolve the reactions.

A: Acetic a hydride with ammonia gives amide.  Lactum with lialh4 gives amine and alcohol

Q: Arrange the following compounds in an increasing order of their reactivity in nucleophilic addition…

A: Given, ethanal, propanal, propanone, butanone.

Q: A) In the boxes provided, rank the following in order of basicity (ability to react with H*). 1 =…

A: More stable anion have less basic character and less stable  anion have more basic character

Q: Which of the following will have the strongest acid-base interaction with NH3? a. BH3 b. BMe3 c.…

A: Fluorine is more electronegative than hydrogen, so due to inductive effects, the electron density…

Q: Rank the following compounds from most reactive to least reactive in an electrophilic aromatic…

A: The reaction in which an electrophile gets substituted to the benzene ring in place of H+ is known…

Q: Rank the following compounds in order of increasing basicity.

A: Since in molecule 2 and molecule 3 we have lone pair electrons of N involved in resonance while in…

Q: 5.3. The following enamine is in equilibrium with which compounds when in trace acidic conditions?…

A: The enamine is in equilibrium with its imine form in presence of trace acidic conditions.

Q: Which of the following functional groups will increase acidity? I. -NO2        II.  -CH2CH3…

A: Which of the following functional groups will increase acidity?

Q: The following enamine is in equilibrium with which compounds when in trace acidic conditions? a.…

A: Enamines are the compounds that are unsaturated and are obtained by the condensation reactions of…

Q: Arrange the following molecules in increasing order of acidity. Base it only on their structural…

A: Bronsted Lowery theory: Acid: The substance which donates proton is an acid. Base: The substance…

Q: Rank each set of compounds in order of increasing basicity.aniline, p-methylaniline, p-nitroaniline

A: Among the given set of compounds, p-nitroaniline has the lowest basicity because it contains phenyl…

Aldehydes and Ketones

Aldehydes and ketones are organic compounds that have a carbonyl group, C = O, as their functional group. They both differ in the placement of this carbonyl group in their structures.