Answer:
Since the repulsions on the bond pairs in H2O molecule are greater than that in NH3, the bond angle in water is less than that of ammonia...
Answer:
base
Explanation:
carbonic acid - H2CO3 - is a weak acid. Therefore, HCO3 itself is its conjugate base. The Na(sodium) ion is neutral.
This means that NaHCO3 is a base. (a weak one)
Answer:
Axial position
Explanation:
In the reduction of 4-tert-butylcyclohexanone with sodium borohydride, the major product has the tert-butyl group in the equatorial position and the alcohol in the axial position.
The reason for this is that, axial bonds are parallel to each other. If substituents are larger than hydrogen, they experience a greater steric crowding in axial compared to the equatorial position. Therefore, many substituted cyclohexane compounds prefer a conformation in which the larger substituents are in equatorial position.
Acetone has α-hydrogens (on both sides) and thus can be deprotonated to give a nucleophilic enolate anion. The aldehyde carbonyl is much more electrophilic than that of a ketone, and therefore reacts rapidly with the enolate.
<h3>What is nitrobenzaldehyde?</h3>
- Synthesis. The synthesis of 3-nitrobenzaldehyde is achieved via nitration of benzaldehyde, which yields especially the meta-isomer. Creation allocation is about 19% for the ortho-, 72% for the meta- and 9% for the para isomers.
- Acetone, propanone, or dimethyl ketone, is an organic combination with the formula (CH3)2CO. It is the easiest and smallest ketone. It is a colorless, highly volatile, and combustible liquid with a characteristic aromatic odor.
- Nitration of benzene with conc nitric acid and conc sulphuric acid gives nitrobenzene. Chlorination with chlorine in the existence of anhydrous aluminum chloride gives meta nitro chlorobenzene.
To learn more about sulphuric acid, refer to:
brainly.com/question/4018599
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