Carbonyl in a sentence

(1) Dinitrogen, bond with a metal carbonyl complex.

(2) The pyruvic acid molecule contains a carbonyl group.

(3) Carbinols can be oxidized to form carbonyl compounds.

(4) The chromophore in this compound is a carbonyl group.

(5) The carbonyl group is often found in natural products.

(6) Carbonyl compounds can undergo rearrangement reactions.

(7) Carbonyl compounds are widely used in organic chemistry.

(8) The carbon chain in aldehydes contains a carbonyl group.

(9) The carbonyl group is susceptible to nucleophilic attack.

(10) Aprotic solvents are commonly used in carbonyl chemistry.

Carbonyl sentence

(11) The carbonyl group is susceptible to reduction reactions.

(12) Carbonyl compounds can undergo reduction to form alcohols.

(13) Carbonyl compounds are commonly found in natural products.

(14) Acyls are organic compounds that contain a carbonyl group.

(15) The carbonyl group is highly reactive towards nucleophiles.

(16) The carbonyl group is commonly found in carbonyl compounds.

(17) Ketones are organic compounds that contain a carbonyl group.

(18) Carbonyls are organic compounds containing a carbonyl group.

(19) The carbonyl group is responsible for the color of many dyes.

(20) The chemical structure of amidones includes a carbonyl group.

Carbonyl make sentence

(21) Carbonyl compounds can be synthesized through various methods.

(22) Aldehydes are organic compounds that contain a carbonyl group.

(23) The carbon chain in ketones has a carbonyl group in the middle.

(24) Ureides are organic compounds that contain two carbonyl groups.

(25) Quinones are organic compounds that contain two carbonyl groups.

(26) Ozonides can be used to convert alkenes into carbonyl compounds.

(27) The carbonyl group undergoes reduction to form an alcohol group.

(28) Carbonyl functional groups can be found in aldehydes and ketones.

(29) The carbonyl group is often found in compounds with strong odors.

(30) Diols can undergo oxidation reactions to form carbonyl compounds.

Sentence of carbonyl

(31) Enamines can be used as protecting groups for carbonyl compounds.

(32) The carbonyl group is a key functional group in organic chemistry.

(33) Carbonyl compounds can undergo oxidation to form carboxylic acids.

(34) The carbonyl group is responsible for the taste of many aldehydes.

(35) Ketoximes can be used as protecting groups for carbonyl compounds.

(36) Aldoximes can be used as protecting groups for carbonyl compounds.

(37) A Bronsted acid can react with a carbonyl compound to form an enol.

(38) The aldehyde compound is known to have a carbonyl functional group.

(39) Carbonyl compounds can be used as solvents in certain applications.

(40) The carbonyl group is a common feature in pharmaceutical compounds.

Carbonyl meaningful sentence

(41) Carbonyl compounds can be used as ligands in coordination chemistry.

(42) Carbonyl compounds can be classified as either aliphatic or aromatic.

(43) The substituents on the carbonyl group affect the compound's acidity.

(44) The protonation of the carbonyl group increased its electrophilicity.

(45) The addition of ethoxide to a carbonyl group can form an enolate ion.

(46) The carbonyl group can be reduced to an alcohol using reducing agents.

(47) The presence of a carbonyl group gives a compound specific properties.

(48) Carbinols can be obtained through the reduction of carbonyl compounds.

(49) Quinone is a class of organic compounds that contain a carbonyl group.

(50) The carbonyl group is found in many important pharmaceutical compounds.

Carbonyl sentence examples

(51) The alkoxide ion can react with carbonyl compounds to form hemiacetals.

(52) The amidin reagent was used to detect the presence of a carbonyl group.

(53) The enol tautomer of a carbonyl compound can be stabilized by resonance.

(54) Carbonyl compounds are often used as intermediates in organic synthesis.

(55) The carbonyl group is often found in compounds with high boiling points.

(56) Hydroxylamine is known for its ability to react with carbonyl compounds.

(57) Amide bonds are formed when a carbonyl group reacts with an amine group.

(58) The carbonyl group is a versatile functional group in organic chemistry.

(59) The carbonyl group is a functional group found in many organic compounds.

(60) The addition of acetylide to a carbonyl compound forms a metal acetylide.

Sentence with carbonyl

(61) Hydroxylamines are known to react with carbonyl compounds to form oximes.

(62) Nucleophiles can react with carbonyl compounds to form imines or enamines.

(63) Many reactions involve the addition of nucleophiles to carbonyl compounds.

(64) Carbonyl compounds can be detected using various spectroscopic techniques.

(65) Carbonyl compounds can be used as catalysts in various chemical reactions.

(66) Aldoximes can be used as reagents for the detection of carbonyl compounds.

(67) Quinones are a class of organic compounds that contain two carbonyl groups.

(68) The acetoacetic acid molecule contains a carbonyl group and a methyl group.

(69) The carbonyl group is often used as a functional group in organic synthesis.

(70) The anhydride molecule consists of two carbonyl groups bonded to each other.

Use carbonyl in a sentence

(71) The carbonyl group is responsible for the characteristic smell of aldehydes.

(72) The oxidation of vicinal diols with periodic acid yields carbonyl compounds.

(73) Alkoxides can react with carbonyl compounds to form hemiacetals and acetals.

(74) The imino group can also be converted to a carbonyl group through oxidation.

(75) The carbonyl group consists of a carbon atom double bonded to an oxygen atom.

(76) Compounds containing a carbonyl group can undergo various chemical reactions.

(77) The benzoyl group is composed of a benzene ring attached to a carbonyl group.

(78) The carbonyl group consists of a carbon atom double-bonded to an oxygen atom.

(79) The exocyclic carbonyl group participated in intramolecular hydrogen bonding.

(80) The structure of quinone consists of a benzene ring with two carbonyl groups.

Sentence using carbonyl

(81) The carbonyl group can form coordination complexes with transition metal ions.

(82) The carbonyl group is planar due to the double bond between carbon and oxygen.

(83) Borane can react with carbonyl compounds to form boron-containing derivatives.

(84) Electrophiles can react with carbonyl compounds through nucleophilic addition.

(85) Imines can also be hydrolyzed to form a carbonyl compound and a primary amine.

(86) The presence of a carbonyl group gives a compound specific chemical properties.

(87) The polarity of the carbonyl group makes it susceptible to nucleophilic attack.

(88) The carbonyl group can be oxidized to a carboxylic acid using oxidizing agents.

(89) Nucleophiles can react with carbonyl compounds to form new carbon-carbon bonds.

(90) Carbonyl compounds can be converted into esters through reaction with alcohols.

Carbonyl example sentence

(91) The carboxylic functional group is composed of a carbonyl and a hydroxyl group.

(92) The amido functional group contains a nitrogen atom bonded to a carbonyl carbon.

(93) Enamines can be converted back to carbonyl compounds by hydrolysis or reduction.

(94) Oximes can be converted back to carbonyl compounds through hydrolysis reactions.

(95) The benzil molecule consists of two benzene rings connected by a carbonyl group.

(96) The triple bond in ethyne can be cleaved using ozone to form carbonyl compounds.

(97) The amide functional group contains a nitrogen atom bonded to a carbonyl carbon.

(98) The structure of lactone includes a carbonyl group and an oxygen atom in a ring.

(99) The barbituric acid molecule contains two carbonyl groups and one nitrogen atom.

(100) The ethoxide ion attacks the carbonyl carbon in a nucleophilic addition reaction.

Sentence with word carbonyl

(101) The carbonyl group is a key feature in the formation of peptide bonds in proteins.

(102) Enamine formation can be achieved using a variety of amine and carbonyl compounds.

(103) The amide bond is planar due to the resonance stabilization of the carbonyl group.

(104) Electrophilic attack on the carbonyl group results in the formation of a new bond.

(105) The addition of borane to carbonyl compounds results in the formation of alcohols.

(106) Ketoximes are organic compounds that contain a nitrogen atom and a carbonyl group.

(107) The carbonyl group is often used as a spectroscopic probe in infrared spectroscopy.

(108) Carbonylating is a versatile method for introducing carbonyl groups into molecules.

(109) Ketoacids are organic compounds that contain a carbonyl group and a carboxyl group.

(110) The carbonylating reaction involves the addition of a carbonyl group to a molecule.

Sentence of carbonyl

(111) Hemiacetals can undergo hydrolysis to regenerate the carbonyl compound and alcohol.

(112) The synthesis of azines involves the reaction of hydrazine with carbonyl compounds.

(113) The amination of carbonyl compounds can lead to the formation of imines or enamines.

(114) The carbon-carbon triple bond in alkynes can be oxidized to form carbonyl compounds.

(115) The addition reaction of a Grignard reagent to a carbonyl compound forms an alcohol.

(116) The amide group is planar due to the resonance stabilization of the carbonyl oxygen.

(117) The oxidation of alcohols to carbonyl compounds can be achieved using periodic acid.

(118) The structure of benzil consists of two benzene rings connected by a carbonyl group.

(119) The formation of oxime is a useful tool in the identification of carbonyl compounds.

(120) The carbonyl group is a key feature in the synthesis of pharmaceutical intermediates.

Carbonyl used in a sentence

(121) The reactivity of carbonyl compounds can be modified by the presence of substituents.

(122) The structure of benzils consists of two benzene rings connected by a carbonyl group.

(123) Imines can undergo hydrolysis to yield the corresponding amine and carbonyl compound.

(124) The synthesis of diazine involves the reaction of hydrazine with a carbonyl compound.

(125) The carbonyl group is often used as a starting material for the synthesis of polymers.

(126) The mechanism of aminolysis involves the attack of an amino group on a carbonyl group.

(127) Carbanions can be generated by the reaction of a carbonyl compound with a strong base.

(128) Periodate is a strong oxidizing agent that can convert alcohols to carbonyl compounds.

(129) The structure of ketene consists of a carbonyl group attached to a double bond carbon.

(130) Open-chain aldehydes and ketones have a carbonyl group at the end of the carbon chain.

Carbonyl sentence in English

(131) The chemical structure of diacetyl includes two carbonyl groups and two methyl groups.

(132) The carboxylic acid group will decarboxylate into a carbonyl group during the reaction.

(133) The chemical structure of esters consists of a carbonyl group bonded to an oxygen atom.

(134) The alkoxide group can undergo nucleophilic addition reactions with carbonyl compounds.

(135) Enamines can be easily converted back to carbonyl compounds by hydrolysis or oxidation.

(136) The carbonyl group is responsible for the characteristic smell of aldehydes and ketones.

(137) The synthesis of hydrazones involves the reaction of a carbonyl compound with hydrazine.

(138) The absorption band in the infrared spectrum indicates the presence of a carbonyl group.

(139) The absorption band at 1700 cm-1 indicates the presence of a carbonyl group in an ester.

(140) The reaction of periodic acid with glycols leads to the formation of carbonyl compounds.

(141) Imine compounds can be hydrolyzed to form the corresponding carbonyl compound and amine.

(142) Enolization is a process that involves the formation of an enol from a carbonyl compound.

(143) The formation of oximes is an important step in the identification of carbonyl compounds.

(144) The addition of organozinc reagents to carbonyl compounds is a common synthetic strategy.

(145) If alicyclics contain a carbonyl group, they can undergo nucleophilic addition reactions.

(146) The imin group can be formed by the reaction of a primary amine with a carbonyl compound.

(147) Nucleophilic attack on a carbonyl group can result in the formation of a new stereocenter.

(148) Carbonyl compounds can be used as starting materials for the synthesis of other compounds.

(149) The stereoselective addition of a nucleophile to a carbonyl compound is a common reaction.

(150) The addition reaction of a nucleophile to a carbonyl group forms a new carbon-oxygen bond.

(151) The reactivity of enamines can be controlled by the choice of amine and carbonyl compound.

(152) The structure of an aldose sugar includes a carbon chain with a carbonyl group at one end.

(153) The addition of acetylide to a carbonyl group can lead to the formation of an enolate ion.

(154) Cyanohydrins can be prepared by the reaction of a carbonyl compound with hydrogen cyanide.

(155) The wavenumber of the infrared absorption band indicated the presence of a carbonyl group.

(156) The chemical structure of chloroacetophenone includes a benzene ring and a carbonyl group.

(157) The structure of benzenecarbonyl consists of a benzene ring with a carbonyl group attached.

(158) The chemist used a Wittig reaction to convert a carbonyl compound into an olefinic product.

(159) The formation of cyanohydrin involves the addition of a cyanide ion to a carbonyl compound.

(160) If an alkoxide is reacted with a carbonyl compound, it may undergo a condensation reaction.

(161) The reactivity of a carbonyl group depends on the nature of the substituents attached to it.

(162) Periodic acid is a powerful oxidizing agent that can convert alcohols to carbonyl compounds.

(163) The bivalences of carbon and oxygen atoms are important in the formation of carbonyl groups.

(164) The synthesis of nitroalkanes involves the reaction of a carbonyl compound with nitric acid.

(165) The formation of an imine involves the reaction of a primary amine with a carbonyl compound.

(166) The carbonyl group is often used as a reactive site for the formation of carbon-carbon bonds.

(167) The formation of cyanohydrin involves the addition of a cyanide group to a carbonyl compound.

(168) The oxidation of vicinal diols to carbonyl compounds can be accomplished using periodic acid.

(169) The ketonic functional group is characterized by a carbonyl group bonded to two carbon atoms.

(170) The carbonyl group can be protected during chemical reactions using various protecting groups.

(171) Nucleophilic attack on a carbonyl group can result in the formation of a hemiacetal or acetal.

(172) The synthesis of enamines involves the reaction of a carbonyl compound with a secondary amine.

(173) The formation of imines involves the reaction between a primary amine and a carbonyl compound.

(174) The synthesis of cyanohydrins involves the addition of hydrogen cyanide to carbonyl compounds.

(175) The synthesis of cyanohydrins involves the addition of hydrogen cyanide to a carbonyl compound.

(176) The synthesis of nitrones involves the reaction of a carbonyl compound with a nitroso compound.

(177) Phenylhydrazine can be used as a test reagent for detecting the presence of carbonyl compounds.

(178) The formation of an enamine involves the nucleophilic addition of an amine to a carbonyl group.

(179) Nucleophilic attack on a carbonyl group can result in the formation of a new carbon-carbon bond.

(180) The peptide bond is formed between the carbonyl carbon and the nitrogen of adjacent amino acids.

(181) The nitro group in nitroalkanes can be converted to a carbonyl group using appropriate reagents.

(182) The alkylations of carbonyl compounds can lead to the formation of alkylated carbonyl compounds.

(183) The lone pair of electrons on the carbon atom in formaldehyde contributes to its carbonyl group.

(184) Enolic compounds can be formed through deprotonation of the alpha-carbon of a carbonyl compound.

(185) Imides are a class of organic compounds that contain a carbonyl group bonded to a nitrogen atom.

(186) The reaction mechanism involves the carboxylic acid group to decarboxylate into a carbonyl group.

(187) The structure of aldehydes includes a carbon atom bonded to a hydrogen atom and a carbonyl group.

(188) The carbonyl group is polar due to the difference in electronegativity between carbon and oxygen.

(189) The chemical group called the carbonyl is responsible for the formation of ketones and aldehydes.

(190) Enolic compounds can be formed by deprotonation of the alpha carbon adjacent to a carbonyl group.

(191) The carbonyl group is often used as a reactive site for the attachment of other functional groups.

(192) The carbonyl group is a versatile functional group that plays a crucial role in organic chemistry.

(193) The amination of carbonyl compounds can be achieved through the use of reagents such as hydrazine.

(194) Carbonylation is a chemical reaction that involves the addition of a carbonyl group to a molecule.

(195) The presence of the carbonyl group in benzenecarbonyl makes it susceptible to nucleophilic attack.

(196) The presence of the carbonyl group in benzenecarbonyl makes it susceptible to oxidation reactions.

(197) The chemical structure of benzophenone consists of two phenyl rings connected by a carbonyl group.

(198) Enolic compounds can be formed through deprotonation of the alpha-hydrogen of a carbonyl compound.

(199) Enolic compounds can be formed through deprotonation of the alpha-position of a carbonyl compound.

(200) The reductant was found to be highly effective in reducing the carbonyl group to an alcohol group.

(201) The formyl group is a functional group that contains a carbonyl group attached to a hydrogen atom.

(202) The reactivity of anhydrides can be influenced by the substituents attached to the carbonyl groups.

(203) The addition of organomagnesium compounds to carbonyl compounds leads to the formation of alcohols.

(204) The peptide bond is formed through a nucleophilic attack of the amino group on the carbonyl carbon.

(205) The absorption band of the compound at 1700 cm-1 corresponds to the stretching of a carbonyl group.

(206) The carbonyl group is responsible for the formation of hemiacetals and acetals in organic chemistry.

(207) The addition of acetylide to a carbonyl compound can lead to the formation of an alkynyl derivative.

(208) The addition of organolithium compounds to carbonyl compounds can lead to the formation of alcohols.

(209) The synthesis of indophenol involves the condensation of an aromatic amine with a carbonyl compound.

(210) The exocyclic carbonyl group in the molecule was responsible for its ability to form hydrogen bonds.

(211) The carbonyl group can be selectively reduced or oxidized in the presence of other functional groups.

(212) The carboxylic acid group can decarboxylate into a carbonyl group under specific reaction conditions.

(213) The halogenation of aldehydes or ketones can lead to the formation of halogenated carbonyl compounds.

(214) The absorption band at 1700 cm-1 indicates the presence of a carbonyl group in an aldehyde or ketone.

(215) The addition of hydrogen cyanide to a carbonyl compound is a common method for preparing cyanohydrins.

(216) The reactivity of cyanohydrins can be modulated by changing the substituents on the carbonyl compound.

(217) The nucleophilic attack of a hydroxide ion on a carbonyl group results in the formation of an alcohol.

(218) The synthesis of quinoxaline involves the condensation of o-phenylenediamine with a carbonyl compound.

(219) Ketoximes can be used as reagents for the determination of carbonyl compounds in analytical chemistry.

(220) The haloform reaction is an important tool for chemists to study the reactivity of carbonyl compounds.

(221) The stability of a hemiacetal depends on the nature of the alcohol and the carbonyl compound involved.

(222) The stereochemistry of an enamine can be controlled by the choice of chiral amine or carbonyl compound.

(223) The carbonyl group is highly polar due to the difference in electronegativity between carbon and oxygen.

(224) The stability of cyanohydrin depends on the nature of the carbonyl compound and the reaction conditions.

(225) The synthesis of hydrazo compounds often involves the condensation of hydrazine with carbonyl compounds.

(226) Periodic acid is a powerful oxidizing agent that can convert alcohols to carbonyl compounds efficiently.

(227) Aldoximes can be converted into nitriles, or they can be hydrolyzed to corresponding carbonyl compounds.

(228) Aldoximes can be transformed into oximes, or they can be hydrolyzed to corresponding carbonyl compounds.

(229) The addition of organomagnesium compounds to carbonyl compounds is a key step in many organic syntheses.

(230) The stability of cyanohydrins depends on the nature of the carbonyl compound and the reaction conditions.

(231) The reactivity of ketones is influenced by the nature of the substituents attached to the carbonyl group.

(232) The addition of organocopper reagents to carbonyl compounds can lead to the formation of copper enolates.

(233) The presence of the carbonyl group in benzenecarbonyl gives it a characteristic infrared absorption peak.

(234) Diketone compounds can exhibit tautomeric behavior, where the position of the carbonyl groups can change.

(235) The reaction between semicarbazide and aldehydes proceeds via nucleophilic addition to the carbonyl group.

(236) The presence of the carbonyl group in benzenecarbonyl allows for its identification through chemical tests.

(237) The absorption band in the infrared spectrum corresponds to the stretching vibrations of the carbonyl group.

(238) Semicarbazide is often used as a reagent for the determination of carbonyl compounds in analytical chemistry.

(239) The addition of organozinc reagents to carbonyl compounds is a common method for forming carbon-carbon bonds.

(240) Hydrazones can be used as reagents in organic synthesis for the selective functionalization of carbonyl compounds.

(241) The addition of organolithium reagents to carbonyl compounds can lead to the formation of new carbon-carbon bonds.

(242) The addition of organolithium compounds to carbonyl compounds can lead to the formation of new carbon-carbon bonds.

(243) If an alkoxide is reacted with a carbonyl compound and a suitable acid, it may undergo a Claisen condensation reaction.

(244) The formation of hydrazones is a common strategy in organic chemistry for the selective detection of carbonyl compounds.

(245) The reactivity of hydrazones can be modulated by the choice of the carbonyl compound and hydrazine used in their synthesis.

(246) Aldoximes are often used as protecting groups for carbonyl compounds, and they can be easily removed under mild conditions.

(247) Aldoximes are often used as protecting groups for carbonyl compounds, and they can be easily cleaved under mild conditions.

(248) The reaction mechanism of esterification involves the nucleophilic attack of the alcohol on the carbonyl carbon of the acid.

(249) Aldoximes, which are commonly used as protecting groups for carbonyl compounds, can be easily removed under mild conditions.

(250) When borohydride is used to reduce a carbonyl group, the reaction typically proceeds with high stereoselectivity and yields.

(251) The reaction between borohydride and a carbonyl compound is typically carried out in a non-aqueous solvent such as ether or THF.

(252) Aldoximes can be transformed into nitro compounds, or they can be subjected to Nef reaction to form corresponding carbonyl compounds.

(253) The reaction between borohydride and a carbonyl compound is typically carried out in the presence of a catalyst such as nickel or palladium.

(254) The carboxyl group is a functional group that contains both a carbonyl group and a hydroxyl group, and it is found in many organic compounds.

(255) Enolates are nucleophilic species that can react with electrophiles, such as carbonyl compounds, which leads to the formation of new carbon-carbon bonds.

(256) Enol ethers are compounds that contain an ether group and an enolizable carbonyl group, which can undergo intramolecular cyclization to form cyclic ethers.

(257) Although the amino group is not directly involved in the formation of peptide bonds, it can influence the reactivity and stability of the adjacent carbonyl group through hydrogen bonding and electrostatic interactions.

The word usage examples above have been gathered from various sources to reflect current and historical usage of the word Carbonyl. They do not represent the opinions of TranslateEN.com.