(Given molar mass in $\text{g mol}^{-1} \, \text{H} : 1, \text{C} : 12, \text{N} : 14, \text{O} : 16$)
The benzoylation reaction involves the synthesis of benzanilide from aniline. The key reaction is:
$ C_6H_5NH_2 + C_6H_5COCl \rightarrow C_6H_5NHCOC_6H_5 + HCl $
Molar masses calculated using the given atomic masses (H: 1, C: 12, N: 14, O: 16) are:
Calculate the moles of aniline used from its given mass:
$ \text{Moles of Aniline} = \frac{\text{Mass}}{\text{Molar Mass}} = \frac{5.8 \, \text{g}}{93 \, \text{g/mol}} $
Based on the reaction stoichiometry (1:1 mole ratio), the theoretical moles of benzanilide equal the moles of aniline. The theoretical mass is:
$ \text{Theoretical Mass} = \left( \frac{5.8}{93} \right) \, \text{mol} \times 197 \, \text{g/mol} $
$ \text{Theoretical Mass} \approx 12.29 \, \text{g} $
The actual mass obtained considers the reaction yield (82%):
$ \text{Actual Mass} = \text{Theoretical Mass} \times \frac{\text{Yield}}{100\%} $
$ \text{Actual Mass} = 12.29 \, \text{g} \times \frac{82}{100} $
$ \text{Actual Mass} \approx 10.07 \, \text{g} $
Rounding the calculated actual mass to the nearest integer gives the final answer:
$ 10.07 \, \text{g} \approx 10 \, \text{g} $
Given below are two statements:
Statement I: The dipole moment of R-CN is greater than R-NC and R-NC can undergo hydrolysis under acidic medium to produce 
Statement II: R-CN hydrolyses under acidic medium to produce a compound which on treatment with $\text{SOCl}_2$, followed by the addition of $\text{NH}_3$ gives another compound(x). This compound (x) on treatment with $\text{NaOCl/NaOH}$ gives a product, that on treatment with $\text{CHCl}_3\text{/KOH/}\Delta$ produces R-NC
In the light of the above statements, choose the correct answer from the options given below
Given below are two statements :
Statement I : Compound (X), shown below, dissolves in $\text{NaHCO}_3$ solution and has two chiral carbon atoms 
Statement II : Compound (Y), shown below, has two carbons with $\text{sp}^3$ hybridization, one carbon with $\text{sp}^2$ and one carbon with $\text{sp}$ hybridization 
In the light of the above statements, choose the correct answer from the options given below :
Given below are two statements:
Statement I: The dipole moment of R-CN is greater than R-NC and R-NC can undergo hydrolysis under acidic medium to produce 
Statement II: R-CN hydrolyses under acidic medium to produce a compound which on treatment with $\text{SOCl}_2$, followed by the addition of $\text{NH}_3$ gives another compound(x). This compound (x) on treatment with $\text{NaOCl/NaOH}$ gives a product, that on treatment with $\text{CHCl}_3\text{/KOH/}\Delta$ produces R-NC
In the light of the above statements, choose the correct answer from the options given below