Answer:
The glycosylation reaction or glycoside formation is an organic reaction in which the hemiacetal group of cyclists ketoses or aldoses turns into acetals, named glycosides. Reaction in the attached picture.
Explanation:
Carbohydrates can be found in an open-chain form or a cyclic form. For the second one, the carbonyl group of the aldehyde could react with the alcohol group of the molecule to form the cycle. As shown in the attached picture, the alcohol group of this cyclic form could react with an alcohol (like methanol) in acidic conditions to form an acetal. These compounds are stable at neutral and acidic conditions, but they hydrolyze at basic conditions. This reaction produces both acetals anomers (α and β) because the attack of the nucleophile (alcohol) could be from both sides. However, the most stable anomer will predominate.
Answer:
D. cis-2-pentene (looks like a frying pan)
Explanation:
pentane looks lihe the letter M
2-methylpentane looks like YV
2-pentyne looks like an upside down L
Answer:
21.86582KJ
Explanation:
The graphical form of the Arrhenius equation is shown on the image attached. Remember that in the Arrhenius equation, we plot the rate constant against the inverse of temperature. The slope of this graph is the activation energy and its y intercept is the frequency factor.
Applying the equation if a straight line, y=mx +c, and comparing the given equation with the graphical form of the Arrhenius equation shown in the image attached, we obtain the activation energy of the reaction as shown.
Answer:
F = 800 N
Explanation:
Given data:
Mass = 80 Kg
Acceleration = 10 m/s²
Force = ?
Solution:
Formula:
<em>F = m × a
</em>
F = force
m = mass
a = acceleration
Now we will put the values in formula:
<em>F = m × a
</em>
F = 80 kg <em>× </em>10 m/s²
F = 800 kg.m/s²
kg.m/s² = N
F = 800 N
