Answer: Option (c) is the correct answer.
Explanation:
Backbone in a nucleic acids strand is made up of sugar molecules attached with phosphodiester bond.
This sugar-phosphate linkage helps in joining of nucleotides in a DNA sequence. Due to this backbone structural framework of nucleotides is formed. In DNA, the sugar is deoxyribose.
Thus, we can conclude that the backbone in a nucleic acids strand is called sugar backbone.
Phosphorous has three lone electrons that need pairing. Similar to how carbon has 4 lone electrons, and forms CH4
To determine the empirical formula and the molecular formula of the compound, we assume a basis of the compound of 100 g. We do as follows:
Mass Moles
K 52.10 52.10/39.10 = 1.33 1.33/1.32 ≈ 1
C 15.8 15.8/12 = 1.32 1.32/1.32 ≈ 1
O 32.1 32.1 / 16 = 2.01 2.01/1.32 ≈ 1.5
The empirical formula would most likely be KCO.
The molecular formula would be K2C2O3.
The answer is “Only some of the molecules of a weak base dissociate to produce hydroxide ions when mixed with water, but all of the molecules of a strong base dissociate to produce hydroxide ions”
Answer:
see explanation below
Explanation:
You are missing the reaction scheme, but in picture 1, I found a question very similar to this, and after look into some other pages, I found the same scheme reaction, so I'm gonna work on this one, to show you how to solve it. Hopefully it will be the one you are asking.
According to the reaction scheme, in the first step we have NaNH2/NH3(l). This reactant is used to substract the most acidic hydrogen in the alkine there. In this case, it will substract the hydrogen from the carbon in the triple bond leaving something like this:
R: cyclopentane
R - C ≡ C (-)
Now, in the second step, this new product will experiment a SN2 reaction, and will attack to the CH3 - I forming another alkine as follow:
R - C ≡ C - CH3
Finally in the last step, Na in NH3 are reactants to promvove the hydrogenation of alkines. In this case, it will undergo hydrogenation in the triple bond and will form an alkene:
R - CH = CH - CH3
In picture 2, you have the reaction and mechanism.