Answer:
cis-1-tert-butyl-3-methylcyclohexane will have a higher percentage of the diequatorial-substituted conformer when compared with the diaxialsubstituted conformer.
Explanation:
The two compound contain or have high stability with the substituent group is at equatorial position but the tert-betyl group in cis-1-tert-butyl-3-methylcyclohexane is larger than the methyl group in trans-1,4-dimethylcyclohexane.
Thus, the equatorial position will be more favorable for the substituent group in the cis-1-tert-butyl-3-methylcyclohexane, therefore having higher percentage of the diequatorial substituted conformer compared with that of diaxial-substituted conformer.
<span>37.9968064 ± 0.0000010 g/mol</span>
2.83 days into hours = 2.83 x 24 = 67.92 hours
67.92 hours into minute = 67.92 x 60 = 4075.2 minutes
4075.2 minutes into seconds = 4075.2 x 60 = 244,512 seconds.
Answer:
1. When observing a positive test for the jones reagent and negative for the Lucas test, it indicates that it is in the presence of a primary alcohol.
Jones reagent behaves like a strong oxidant, where it transforms the primary alcohols into carboxylic acids and the secondary alcohols into ketones. Tertiary alcohols do not react.
With the Lucas test, tertiary alcohols react immediately producing turbidity, while secondary alcohols do so in five minutes. Primary alcohols do not react significantly with Lucas reagent at room temperature.
2. No reaction (See the attached drawing)
3. (see the attached drawing)
The pairs are:
K, Kr - Same period
Be, Mg - Same group
Ni, Tc - Both are transition metals
B, Ge - Both are metaloids
Al, Pb - Both form inert oxides
