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Read the passage given below and answer the following questions:Greater is the stability of the substituted ammonium cation, stronger should be the corresponding amine as a base. Thus, the order of basicity of aliphatic amines should be: primary > secondary > tertiary, which is opposite to the inductive effect based order. Secondly, when the alkyl group is small, like –CH3 group, there is no steric hindrance to H-bonding. In case the alkyl group is bigger than CH3 group, there will be steric hinderance to H-bonding. Therefore, the change of nature of the alkyl group, e.g., from –CH3 to –C2H5 results in change of the order of basic strength.In the following questions a statement of assertion followed by a statement of reason is given. Choose the correct answer out of the following choices.Assertion (A): (CH3)2NH > CH3NH2 > (CH3)3N > NH3 is the order of basic strength in case of methyl substituted amines.Reason (R): The inductive effect, solvation effect and steric hindrance of the alkyl group decides the basic strength of alkyl amines in the aqueous state.a)Assertion and reason both are correct statements and reason is correct explanation for assertion.b)Assertion and reason both are correct statements but reason is not correct explanation for assertion.c)Assertion is correct statement but reason is wrong statement.d)Assertion is wrong statement but reason is correct statement.Correct answer is option 'A'. Can you explain this answer? for Class 12 2024 is part of Class 12 preparation. The Question and answers have been prepared according to the Class 12 exam syllabus. Information about Read the passage given below and answer the following questions:Greater is the stability of the substituted ammonium cation, stronger should be the corresponding amine as a base. Thus, the order of basicity of aliphatic amines should be: primary > secondary > tertiary, which is opposite to the inductive effect based order. Secondly, when the alkyl group is small, like –CH3 group, there is no steric hindrance to H-bonding. In case the alkyl group is bigger than CH3 group, there will be steric hinderance to H-bonding. Therefore, the change of nature of the alkyl group, e.g., from –CH3 to –C2H5 results in change of the order of basic strength.In the following questions a statement of assertion followed by a statement of reason is given. Choose the correct answer out of the following choices.Assertion (A): (CH3)2NH > CH3NH2 > (CH3)3N > NH3 is the order of basic strength in case of methyl substituted amines.Reason (R): The inductive effect, solvation effect and steric hindrance of the alkyl group decides the basic strength of alkyl amines in the aqueous state.a)Assertion and reason both are correct statements and reason is correct explanation for assertion.b)Assertion and reason both are correct statements but reason is not correct explanation for assertion.c)Assertion is correct statement but reason is wrong statement.d)Assertion is wrong statement but reason is correct statement.Correct answer is option 'A'. Can you explain this answer? covers all topics & solutions for Class 12 2024 Exam. Find important definitions, questions, meanings, examples, exercises and tests below for Read the passage given below and answer the following questions:Greater is the stability of the substituted ammonium cation, stronger should be the corresponding amine as a base. Thus, the order of basicity of aliphatic amines should be: primary > secondary > tertiary, which is opposite to the inductive effect based order. Secondly, when the alkyl group is small, like –CH3 group, there is no steric hindrance to H-bonding. In case the alkyl group is bigger than CH3 group, there will be steric hinderance to H-bonding. Therefore, the change of nature of the alkyl group, e.g., from –CH3 to –C2H5 results in change of the order of basic strength.In the following questions a statement of assertion followed by a statement of reason is given. Choose the correct answer out of the following choices.Assertion (A): (CH3)2NH > CH3NH2 > (CH3)3N > NH3 is the order of basic strength in case of methyl substituted amines.Reason (R): The inductive effect, solvation effect and steric hindrance of the alkyl group decides the basic strength of alkyl amines in the aqueous state.a)Assertion and reason both are correct statements and reason is correct explanation for assertion.b)Assertion and reason both are correct statements but reason is not correct explanation for assertion.c)Assertion is correct statement but reason is wrong statement.d)Assertion is wrong statement but reason is correct statement.Correct answer is option 'A'. Can you explain this answer?.

Solutions for Read the passage given below and answer the following questions:Greater is the stability of the substituted ammonium cation, stronger should be the corresponding amine as a base. Thus, the order of basicity of aliphatic amines should be: primary > secondary > tertiary, which is opposite to the inductive effect based order. Secondly, when the alkyl group is small, like –CH3 group, there is no steric hindrance to H-bonding. In case the alkyl group is bigger than CH3 group, there will be steric hinderance to H-bonding. Therefore, the change of nature of the alkyl group, e.g., from –CH3 to –C2H5 results in change of the order of basic strength.In the following questions a statement of assertion followed by a statement of reason is given. Choose the correct answer out of the following choices.Assertion (A): (CH3)2NH > CH3NH2 > (CH3)3N > NH3 is the order of basic strength in case of methyl substituted amines.Reason (R): The inductive effect, solvation effect and steric hindrance of the alkyl group decides the basic strength of alkyl amines in the aqueous state.a)Assertion and reason both are correct statements and reason is correct explanation for assertion.b)Assertion and reason both are correct statements but reason is not correct explanation for assertion.c)Assertion is correct statement but reason is wrong statement.d)Assertion is wrong statement but reason is correct statement.Correct answer is option 'A'. Can you explain this answer? in English & in Hindi are available as part of our courses for Class 12. Download more important topics, notes, lectures and mock test series for Class 12 Exam by signing up for free.

Here you can find the meaning of Read the passage given below and answer the following questions:Greater is the stability of the substituted ammonium cation, stronger should be the corresponding amine as a base. Thus, the order of basicity of aliphatic amines should be: primary > secondary > tertiary, which is opposite to the inductive effect based order. Secondly, when the alkyl group is small, like –CH3 group, there is no steric hindrance to H-bonding. In case the alkyl group is bigger than CH3 group, there will be steric hinderance to H-bonding. Therefore, the change of nature of the alkyl group, e.g., from –CH3 to –C2H5 results in change of the order of basic strength.In the following questions a statement of assertion followed by a statement of reason is given. Choose the correct answer out of the following choices.Assertion (A): (CH3)2NH > CH3NH2 > (CH3)3N > NH3 is the order of basic strength in case of methyl substituted amines.Reason (R): The inductive effect, solvation effect and steric hindrance of the alkyl group decides the basic strength of alkyl amines in the aqueous state.a)Assertion and reason both are correct statements and reason is correct explanation for assertion.b)Assertion and reason both are correct statements but reason is not correct explanation for assertion.c)Assertion is correct statement but reason is wrong statement.d)Assertion is wrong statement but reason is correct statement.Correct answer is option 'A'. Can you explain this answer? defined & explained in the simplest way possible. Besides giving the explanation of Read the passage given below and answer the following questions:Greater is the stability of the substituted ammonium cation, stronger should be the corresponding amine as a base. Thus, the order of basicity of aliphatic amines should be: primary > secondary > tertiary, which is opposite to the inductive effect based order. Secondly, when the alkyl group is small, like –CH3 group, there is no steric hindrance to H-bonding. In case the alkyl group is bigger than CH3 group, there will be steric hinderance to H-bonding. Therefore, the change of nature of the alkyl group, e.g., from –CH3 to –C2H5 results in change of the order of basic strength.In the following questions a statement of assertion followed by a statement of reason is given. Choose the correct answer out of the following choices.Assertion (A): (CH3)2NH > CH3NH2 > (CH3)3N > NH3 is the order of basic strength in case of methyl substituted amines.Reason (R): The inductive effect, solvation effect and steric hindrance of the alkyl group decides the basic strength of alkyl amines in the aqueous state.a)Assertion and reason both are correct statements and reason is correct explanation for assertion.b)Assertion and reason both are correct statements but reason is not correct explanation for assertion.c)Assertion is correct statement but reason is wrong statement.d)Assertion is wrong statement but reason is correct statement.Correct answer is option 'A'. Can you explain this answer?, a detailed solution for Read the passage given below and answer the following questions:Greater is the stability of the substituted ammonium cation, stronger should be the corresponding amine as a base. Thus, the order of basicity of aliphatic amines should be: primary > secondary > tertiary, which is opposite to the inductive effect based order. Secondly, when the alkyl group is small, like –CH3 group, there is no steric hindrance to H-bonding. In case the alkyl group is bigger than CH3 group, there will be steric hinderance to H-bonding. Therefore, the change of nature of the alkyl group, e.g., from –CH3 to –C2H5 results in change of the order of basic strength.In the following questions a statement of assertion followed by a statement of reason is given. Choose the correct answer out of the following choices.Assertion (A): (CH3)2NH > CH3NH2 > (CH3)3N > NH3 is the order of basic strength in case of methyl substituted amines.Reason (R): The inductive effect, solvation effect and steric hindrance of the alkyl group decides the basic strength of alkyl amines in the aqueous state.a)Assertion and reason both are correct statements and reason is correct explanation for assertion.b)Assertion and reason both are correct statements but reason is not correct explanation for assertion.c)Assertion is correct statement but reason is wrong statement.d)Assertion is wrong statement but reason is correct statement.Correct answer is option 'A'. Can you explain this answer? has been provided alongside types of Read the passage given below and answer the following questions:Greater is the stability of the substituted ammonium cation, stronger should be the corresponding amine as a base. Thus, the order of basicity of aliphatic amines should be: primary > secondary > tertiary, which is opposite to the inductive effect based order. Secondly, when the alkyl group is small, like –CH3 group, there is no steric hindrance to H-bonding. In case the alkyl group is bigger than CH3 group, there will be steric hinderance to H-bonding. Therefore, the change of nature of the alkyl group, e.g., from –CH3 to –C2H5 results in change of the order of basic strength.In the following questions a statement of assertion followed by a statement of reason is given. Choose the correct answer out of the following choices.Assertion (A): (CH3)2NH > CH3NH2 > (CH3)3N > NH3 is the order of basic strength in case of methyl substituted amines.Reason (R): The inductive effect, solvation effect and steric hindrance of the alkyl group decides the basic strength of alkyl amines in the aqueous state.a)Assertion and reason both are correct statements and reason is correct explanation for assertion.b)Assertion and reason both are correct statements but reason is not correct explanation for assertion.c)Assertion is correct statement but reason is wrong statement.d)Assertion is wrong statement but reason is correct statement.Correct answer is option 'A'. Can you explain this answer? theory, EduRev gives you an ample number of questions to practice Read the passage given below and answer the following questions:Greater is the stability of the substituted ammonium cation, stronger should be the corresponding amine as a base. Thus, the order of basicity of aliphatic amines should be: primary > secondary > tertiary, which is opposite to the inductive effect based order. Secondly, when the alkyl group is small, like –CH3 group, there is no steric hindrance to H-bonding. In case the alkyl group is bigger than CH3 group, there will be steric hinderance to H-bonding. Therefore, the change of nature of the alkyl group, e.g., from –CH3 to –C2H5 results in change of the order of basic strength.In the following questions a statement of assertion followed by a statement of reason is given. Choose the correct answer out of the following choices.Assertion (A): (CH3)2NH > CH3NH2 > (CH3)3N > NH3 is the order of basic strength in case of methyl substituted amines.Reason (R): The inductive effect, solvation effect and steric hindrance of the alkyl group decides the basic strength of alkyl amines in the aqueous state.a)Assertion and reason both are correct statements and reason is correct explanation for assertion.b)Assertion and reason both are correct statements but reason is not correct explanation for assertion.c)Assertion is correct statement but reason is wrong statement.d)Assertion is wrong statement but reason is correct statement.Correct answer is option 'A'. Can you explain this answer? tests, examples and also practice Class 12 tests.