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For the compound A-CH(2)-CH(27)-A draw t...

For the compound `A-CH_(2)-CH_(27)-A` draw the newman projection formula of all the stable conformational it `mu_(obs) = 2D " and " X_(anti) = 0.75 " then find " mu_(gauche.)("If "A= NO_(2))`

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To solve the problem step by step, we will first address the drawing of the Newman projection for the compound \( A-CH_2-CH_2-A \) and then calculate \( \mu_{\text{gauche}} \) based on the given data. ### Step 1: Understand the Compound Structure The compound can be represented as \( A-CH_2-CH_2-A \), where \( A \) is a substituent (in this case, \( NO_2 \)). The two \( CH_2 \) groups are connected to the substituents \( A \). ### Step 2: Draw the Newman Projection To draw the Newman projection, we will look down the bond connecting the two \( CH_2 \) groups. The three main conformations to consider are: 1. **Eclipsed Conformation**: In this conformation, the substituents on the front and back carbon atoms are aligned with each other. 2. **Gauche Conformation**: In this conformation, the substituents are staggered but not opposite each other (i.e., they are at a dihedral angle of 60 degrees). 3. **Anti Conformation**: In this conformation, the substituents are staggered and positioned opposite each other (i.e., at a dihedral angle of 180 degrees). #### Eclipsed Conformation - Draw the \( NO_2 \) groups on the front and back carbon atoms aligned with each other. - The remaining positions will have hydrogen atoms. #### Gauche Conformation - Draw the \( NO_2 \) groups staggered at a 60-degree angle relative to each other. - The remaining positions will have hydrogen atoms. #### Anti Conformation - Draw the \( NO_2 \) groups staggered and directly opposite each other. - The remaining positions will have hydrogen atoms. ### Step 3: Label the Conformations - Label the first conformation as **Eclipsed**. - Label the second conformation as **Gauche**. - Label the third conformation as **Anti**. ### Step 4: Calculate \( \mu_{\text{gauche}} \) Given: - \( \mu_{\text{obs}} = 2D \) - \( X_{\text{anti}} = 0.75 \) Using the formula: \[ \mu_{\text{obs}} = \mu_{\text{gauche}} \cdot X_{\text{gauche}} + \mu_{\text{anti}} \cdot X_{\text{anti}} \] Since \( X_{\text{gauche}} + X_{\text{anti}} = 1 \), we can find \( X_{\text{gauche}} \): \[ X_{\text{gauche}} = 1 - X_{\text{anti}} = 1 - 0.75 = 0.25 \] Substituting the known values into the equation: \[ 2 = \mu_{\text{gauche}} \cdot 0.25 + 0 \cdot 0.75 \] \[ 2 = \mu_{\text{gauche}} \cdot 0.25 \] Now, solving for \( \mu_{\text{gauche}} \): \[ \mu_{\text{gauche}} = \frac{2}{0.25} = 8D \] ### Final Answer The value of \( \mu_{\text{gauche}} \) when \( A = NO_2 \) is \( 8D \).
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It is given that for conformational isomers, the net dipole moment mu_(obs)=sum mu_(i)x_(i) Where mu_(obs) = obsereved dipole moment of the compound mu_(i) = dipole moment of the stable conformational isomers X_(1) = mole fraction of stable conformers of the compound Z-CH_(2)-CH_(2)-Z draw the Newman projection formula of all stable conformational isomers, if mu_(obs) = 1D, " and " X_(anti) = 0.82, " find " mu_(gauche) . Now draw the Newman projection formula of the most stable conformation of meso Y-CHD-CHD-Y. (a) If Y is CH_(3) ("rotation about "C_(2)-C_(3) " bond") (b) If Y is OH ("rotation about "C_(1)-C_(2) " bond")

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Knowledge Check

  • The empirical formula of the compound is CH_(2)O , the possible molecular formula can be

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    B
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    C
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