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The reaction of 2-phenyl-3-bromopentane with NaNH2 will result in an elimination reaction where a hydrogen atom is removed from the beta position, leading to the formation of an alkyne.

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1y ago

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What is the product when C5H10Br2 reacts with NaNH2 in liquid ammonia?

The reaction between C5H10Br2 and NaNH2 in liquid ammonia results in the formation of a diene compound known as 1,5-hexadiene. The NaNH2 acts as a strong base and abstracts a proton from the dihalide compound, leading to the formation of the diene product.


Is NaNh2 a strong base?

Yes


How does the reaction between NaNH2 and CH3I proceed?

The reaction between NaNH2 and CH3I proceeds through a nucleophilic substitution reaction, where the NaNH2 acts as a nucleophile attacking the carbon atom in CH3I, leading to the formation of a new compound and the release of sodium iodide as a byproduct.


If NaNH2 is dissolved in liquid ammonia it is an acid or a base?

Well ammonia is a weak base and and NaNH2 is a strong base, so overall, you've got a pretty strong base.


If NaNH2 is dissolved in liquid ammonia is it an acid or a base?

Well ammonia is a weak base and and NaNH2 is a strong base, so overall, you've got a pretty strong base.


What is the mechanism of the reaction involving nanh2 and nh3?

The reaction involving NaNH2 and NH3 is a nucleophilic substitution reaction. In this reaction, the NaNH2 acts as a strong base and replaces a hydrogen atom in NH3, forming a new compound. This reaction is commonly used in organic synthesis to introduce new functional groups into molecules.


Does NaNH2 dissolve in water?

Yes, NaNH2 (sodium amide) is highly soluble in water due to its ionic nature. When dissolved in water, it dissociates into sodium ions (Na+) and amide ions (NH2-) which are stabilized by hydration.


WHY is NaNH2 a base?

NaNH2 is a base because it can accept a proton (H+) from an acid to form ammonia (NH3) and the conjugate base of the acid. This reaction results in the formation of NH4+ and N3- ions, showing the ability of NaNH2 to accept protons and act as a base.


What is the products when pyridine reacts with sodamide and pyrrolidine?

When pyridine reacts with sodamide (NaNH2) and pyrrolidine, it forms a C-N bond cleavage product by replacing the nitrogen atom of the pyridine ring with the amide group from sodamide. The resulting product is a pyridine with an amide group attached to its carbon atom.


Is NaNH2 ionic or covalent?

NaNH2 is considered an ionic compound because it is composed of a metal (Na) and a nonmetal (NH2). The sodium (Na) atom donates an electron to the NH2 group, forming Na+ and NH2- ions.


What do you get when NaNH2 is dissolved in an alcohol?

When NaNH2 is dissolved in an alcohol, it acts as a strong base that can deprotonate the alcohol molecule on its α-carbon, forming an alkoxide ion. This alkoxide ion can undergo further reactions like nucleophilic substitution or elimination reactions.


What is the empirical formula for Sodiumamide?

According to wikipedia, the formula is: 2 Na + 2 NH3 → 2 NaNH2 + H2 I hope I helped! ;)