Answer:
The correct answer is vertebrate enzyme hydrolyze alpha-1,4 glycosidic linkage but not glucose in the beta configuration.
Explanation:
The amylase that is present inside human body is called salivary alpha amylase,an enzyme that digest the alpha-1,4-glycosidic linkages of starch but does not act on those glycosidic linkages which are present in beta configuration.
Cellulose contain beta-1,4-glycosidic linkages.That"s why it is not digested by the alpha amylase enzyme present inside the human body basically present in the saliva.
1) We need to convert 12.0 g of H2 into moles of H2, and <span> 74.5 grams of CO into moles of CO
</span><span>Molar mass of H2: M(H2) = 2*1.0= 2.0 g/mol
Molar mass of CO: M(CO) = 12.0 +16.0 = 28.0 g/mol
</span>12.0 g H2 * 1 mol/2.0 g = 6.0 mol H2
74.5 g CO * 1 mol/28.0 g = 2.66 mol CO
<span>2) Now we can use reaction to find out what substance will react completely, and what will be leftover.
CO + 2H2 -------> CH3OH
1 mol 2 mol
given 2.66 mol 6 mol (excess)
How much
we need CO? 3 mol 6 mol
We see that H2 will be leftover, because for 6 moles H2 we need 3 moles CO, but we have only 2.66 mol CO.
So, CO will react completely, and we are going to use CO to find the mass of CH3OH.
3) </span>CO + 2H2 -------> CH3OH
1 mol 1 mol
2.66 mol 2.66 mol
4) We have 2.66 mol CH3OH
Molar mass CH3OH : M(CH3OH) = 12.0 + 4*1.0 + 16.0 = 32.0 g/mol
2.66 mol CH3OH * 32.0 g CH3OH/ 1 mol CH3OH = 85.12 g CH3OH
<span>
Answer is </span>D) 85.12 grams.
<h3><u>Full Question:</u></h3>
The following compound has been found effective in treating pain and inflammation (J. Med. Chem. 2007, 4222). Which sequence correctly ranks each carbonyl group in order of increasing reactivity toward nucleophilic addition?
A) 1 < 2 < 3
B) 2 < 3 < 1
C) 3 < 1 < 2
D) 1 < 3 < 2
<h3><u>Answer: </u></h3>
The rate of nucleophilic attack of carbonyl compounds is 2<3 <1.
Option B
<h3><u>Explanation. </u></h3>
Nucleophilic attack is explained as the attack of an electron rich radical to a carbonyl compound like aldehyde or a ketone. A nucleophile has a high electron density, so it searches for a electropositive atom where it can donate a portion of its electron density and become stable.
A carbonyl compound is a 
hybridized carbon atom with a double bonded oxygen atom in it. The oxygen atom pulls a huge portion of electron density from carbon being very electropositive.
In a ketone, there are two factors that make it less likely to undergo a nucleophilic attack than aldehyde. Firstly, the steric hindrance of two carbon groups being attached with the carbonyl carbon makes it harder for the nucleophile to approach. Secondly, the electron push by the carbon groups attached makes the carbonyl carbon a bit less electropositive than the aldehyde one. So aldehydes are more reactive towards a nucleophilic addition reaction.
Answer:
Don't mark me brainliest because of this but I'm pretty sure your supposed to give us the words because teachers don't give you things like that without the words you will the answer in with.
