The primary cycle of fatty acid synthesis produces a four-carbon acyl group. Every following cycle adds a three-carbon malonyl group, which stretches off one molecule of CO2 (one carbon atom) in a condensation response. Thus, the net number of carbon atoms additional by each following cycle is two. For the reason that the first cycle makes a four-carbon chain, and each added cycle extends the chain by two carbon atoms, the second cycle fallouts in a six-carbon chain, the third cycle fallouts in an eight-carbon chain, and so on. And so, the synthesis of the 14-carbon myristic acid necessitates six repetitions.
Answer:
Each student will need;
1 red jelly bean, 1 white jelly bean, 1 black jelly bean and 3 red jelly beans.
Explanation:
Sodium bicarbonate molecule, NaHCO3, or baking soda is composed of the following:
1 atom of sodium, Na;
1 atom of hydrogen, H;
1 atom of carbon, C, and
3 atoms of oxygen.
For each of the models to be built by the two students, these atoms are to be represented accordingly.
Since Red jelly beans represent sodium atoms (Na), white jelly beans represent hydrogen atoms (H), black jelly beans represent carbon atoms (C), and blue jelly beans represent oxygen atoms (O), each student will need;
1 red jelly bean, 1 white jelly bean, 1 black jelly bean and 3 red jelly beans.
A sample model is found in the attachment below:
Answer: The mass of the gas is 18.3 g/mol.
Explanation:
To calculate the rate of diffusion of gas, we use Graham's Law.
This law states that the rate of effusion or diffusion of gas is inversely proportional to the square root of the molar mass of the gas. The equation given by this law follows:




Squaring both sides and solving for 

Hence, the molar mas of unknown gas is 18.3 g/mol.
Answer:
Atorvastatin has two chiral centers. The question doesn't include the box where have to answer but I can show you in an image where are located and their configuration.
Explanation:
The first image shows the chemical structure of atorvastatin and their chiral centers identified as 1 and 2 respectively.
The second image shows the Fischer projections corresponding to every chiral carbon 1 and 2. I wrote R so suggest that there are more carbon atoms forward but not only corresponds to carbon atoms.
You can see that the chiral carbon 1 has R configuration due to the direction from the main substituent to the second follow the clockwise.
The chiral carbon 2 has S configuration due to the direction from the main substituent to the second one go anticlockwise.
Adhesion describes water's attraction to other substances.
The term Adhesion refers to the tendency of particles or surfaces which are not similar to cling to one another. So basically, the adhesion occurs in water when the water is attracted or cling to other substance not similar to water.