Hi, you have not provided structure of the aldehyde and alkoxide ion.
Therefore i'll show a mechanism corresponding to the proton transfer by considering a simple example.
Explanation: For an example, let's consider that proton transfer is taking place between a simple aldehyde e.g. acetaldehyde and a simple alkoxide base e.g. methoxide.
The hydrogen atom attached to the carbon atom adjacent to aldehyde group are most acidic. Hence they are removed by alkoxide preferably.
After removal of proton from aldehyde, a carbanion is generated. As it is a conjugated carbanion therefore the negative charge on carbon atom can conjugate through the carbonyl group to form an enolate which is another canonical form of the carbanion.
All the structures are shown below.
A test tube of zinc oxide
Answer:
Your correct answer is A. 1,2,1,2
Explanation:
Please mark brainliest!
Answer:
Record players
Explanation:
In a record player, a stylus vibrates as it follows a spiral groove cut into the surface of the rotating record.
The vibrations (analogue) are converted into electrical signals and fed into an amplifier to produce the sounds you hear
Fiber optic cables, Wi-Fi devices, and flat screen TVs use digitized signals to encode and transmit information
Answer:
The smallest unit of a compound is a molecule, which is made up of atoms held together by bonds.