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महाराष्ट्र राज्य शिक्षण मंडळएचएससी विज्ञान (सामान्य) इयत्ता १२ वी

What is the action of the following on ethyl bromide? silver acetate

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प्रश्न

What is the action of the following on ethyl bromide?

silver acetate

Write the chemical reaction for the following:

Ethyl bromide is heated with silver acetate.

रासायनिक समीकरणे/रचना
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उत्तर

\[\ce{\underset{\text{Ethyl bromide}}{C2H5Br} + \underset{\text{Silver acetate}}{CH3COOAg}->\underset{\text{Ethyl acetate}}{CH3COOC2H5} + AgBr}\]

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2018-2019 (March) Set 1

संबंधित प्रश्‍न

How do you convert the following:

Ethanol to propanenitrile


In the following pair of halogen compounds, which compound undergoes a faster SN1 reaction?


Write the structure of the major organic product in the following reaction:

\[\ce{CH3CH2Br + KCN ->[aq{.} ethanol]}\]


What happens when methyl chloride is treated with KCN?


How the following conversion can be carried out?

Ethyl chloride to propanoic acid.


Which would undergo SN2 reaction faster in the following pair and why ?

CH3 – CH2 ​– Br and CH3 ​– CH2 ​– I


What is the action of the following on ethyl bromide?

moist silver oxide


In the reaction, \[\ce{R - X + NaOR' -> ROR’ + X}\] ( – ve ion). The main product formed is:


Arrange the following organic compounds in descending order of their reactivity towards SN1 reaction.

C6H5CH2Br, C6H5CH(C6H5)Br, C6H5CH(CH3)Br, C6H5C(CH3)(C6H5)Br


Which of the following is an example of SN2 reaction?


Which of the following reactions is an example of nucleophilic substitution reaction?


SN2 mechanism proceeds through intervention of ____________.


Tertiary alkyl halides are practically inert to substitution by SN2 mechanism because of ____________.


2-Bromopentane is heated with potassium ethoxide in ethanol. The major product obtained is ____________.


SN1 reaction of alkyl halides lead to ___________.


Compound ‘A’ with molecular formula \[\ce{C4H9Br}\] is treated with aq. \[\ce{KOH}\] solution. The rate of this reaction depends upon the concentration of the compound ‘A’ only. When another optically active isomer ‘B’ of this compound was treated with aq. \[\ce{KOH}\] solution, the rate of reaction was found to be dependent on concentration of compound and \[\ce{KOH}\] both.

(i) Write down the structural formula of both compounds ‘A’ and ‘B’.

(ii) Out of these two compounds, which one will be converted to the product with inverted configuration.


Elimination reactions (especially β-elimination) are as common as the nucleophilic substitution reaction in case of alkyl halides. Specify the reagents used in both cases.


Which one is the correct order of nucleophilic strength (pKa) of following nucleophiles?


In which reaction mechanism carbocation is formed?


The number of chiral alcohol (s) with molecular formula C4H10O is ______.


The major product formed in the following reaction is:


In SN1 reactions, the correct order of reactivity for the following compounds:

CH3Cl, CH3CH2Cl, (CH3)2CHCl and (CH3)3CCl is ______.


Convert bromoethane to propanamine.


The following questions are case-based questions. Read the passage carefully and answer the questions that follow:

Nucleophilic Substitution:
Nucleophilic substitution reaction of haloalkane can be conducted according to both SN1 and SN2 mechanisms. SN1 is a two-step reaction, while SN2 is a single-step reaction. For any haloalkane, which mechanism is followed depends on factors such as the structure of haloalkane, properties of leaving group, nucleophilic reagent and solvent.

Influences of solvent polarity:
In SN1 reaction, the polarity of the system increases from the reactant to the transition state, because a polar solvent has a greater effect on the transition state than the reactant, thereby reducing activation energy and accelerating the reaction. In SN2 reaction, the polarity of the system generally does not change from the reactant to the transition state, and only charge dispersion occurs. At this time, the polar solvent has a great stabilizing effect on Nu than the transition state, thereby increasing activation energy and slow down the reaction rate. For example, the decomposition rate (SN1) of tertiary chlorobutane at 25°C in water (dielectric constant 79) is 300000 times faster than in ethanol (dielectric constant 24).

The reaction rate (SN2) of 2-bromopropane and NaOH in ethanol containing 40% water is twice slower than in absolute ethanol. Hence the level of solvent polarity has an influence on both SN1 and SN2 reactions but with different results. Generally speaking, a weak polar solvent is favourable for SN2 reaction, while a strong polar solvent is favourable for SN1. Generally speaking, the substitution reaction of tertiary haloalkane is based on SN1 mechanism in solvents with a strong polarity (for example ethanol containing water).

Answer the following questions:

(a) Why racemisation occurs in SN1? (1)

(b) Why is ethanol less polar than water? (1)

(c) Which one of, the following in each pair is more reactive towards SN2 reaction? (2)

(i) CH3 – CH2 – I or CH3CH2 – Cl

(ii)

OR

(c) Arrange the following in the increasing order of their reactivity towards SN1 reactions: (2)

(i) 2-Bromo-2-methylbutane, 1-Bromo-pentane, 2-Bromo-pentane

(ii) 1-Bromo-3-methylbutane, 2-Bromo-2-methylbutane, 2-Bromo-3- methylbutane


 Acetic anhydride from acetic acid


HCI, Major product ______.


The compound that will undergo SN1 reaction with the fastest rate is:


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