Answer:
The mechanism of this reaction i shown on the second uploaded image
The final product of the reaction is shown on the third uploaded image
The hydroxide would be first mixed with the ketone group before the aldehyde is added
Explanation:
The compound given in the question is 2,2-dimethylpropanal (pivalaldehyde) the structural formula is shown on the first uploaded image
looking at the structurally formula we can see that the hydroxide promoted reaction of this compound would be between the ketone and aldehyde functional group present in this compound in the presence of a hydroxide
Now this process of the reaction is this
The 
is first made to react with the ketone group
Then the aldehyde is added
What happens is that that the would search for an acidic proton because it is a base and this acidic proton is present in ketone and absent in aldehyde group hence the reason for the first reaction with the ketone group before the aldehyde is added
Answer:
Carbon : chemical symbol is "C"
Chlorine: chemical symbol is"Cl"
Enzymes are characterized to have weak bonds because their tertiary structure could easily bend and break because it will have to adjust to the shape of the substrate. It could be done via induced fitting or lock-and-key theory. These weak bonds are intermolecular forces like the London forces, electrostatic interactions and hydrogen bonding.
Rubbing alcohol is a solution
Answer:
Nitrifying Bacteria are a group of aerobic bacteria important in the nitrogen cycle as converters of soil ammonia to nitrates, compounds usable by plants. An example is nitrosomonas or nitrobacter and species in that family.
The schematic diagram is attached below, which summarises the oxidation of ammonia or free nitrogen in the soil to nitrates for the cowpea plant's utilisation.
