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OLEGan [10]
3 years ago
5

Why can't 1−methylcyclohexanol be prepared from a carbonyl compound by reduction? select the single best answer?

Chemistry
1 answer:
forsale [732]3 years ago
4 0
1−methylcyclohexanol is a tertiary alcohol. Tertiary Alcohols are synthesized by either reacting Ketone with Organometallic compounds like Grignard reagent or by hydration of substituted alkenes. <span>1−methylcyclohexanol can not be synthesized by reduction of carbonyl compound because it is not possible to have a starting carbonyl compound having carbonyl group along with three other alkyl groups (as carbon can only form 4 bonds).

Result:
           Tertiary alcohols don't contain a hydrogen atom at carbon attached to hydroxyl group that is why it is not possible to synthesize </span><span>1−methylcyclohexanol by reduction of carbonyl compound.</span>

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that is   H2SO4  = 2H^+  +  SO4^2-

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What is the enthalpy change (in kj) of a chemical reaction that raises the temperature of 250.0 ml of solution having a density
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Using any data you can find in the ALEKS Data resource, calculate the equilibrium constant K at 30.0 °C for the following reacti
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Answer : The value of K for this reaction is, 2.6\times 10^{15}

Explanation :

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Now put all the given values in this expression, we get:

\Delta G^o=[1mole\times (-389.8kJ/mol)]-[1mole\times (-163.2kJ/mol)+1mole\times (-137.2kJ/mol)]

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The relation between the equilibrium constant and standard Gibbs, free energy is:

\Delta G^o=-RT\times \ln K

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\Delta G^o = standard Gibbs, free energy  = -89.4 kJ/mol = -89400 J/mol

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Thus, the value of K for this reaction is, 2.6\times 10^{15}

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