When two monosaccharides combine to make a disaccharide, water is the byproduct.
<h3>What are monosaccharides ?</h3>
The most fundamental building blocks from which all carbohydrates are constructed are monosaccharides, commonly known as simple sugars. They are the most basic types of sugar. They are typically crystalline solids, colorless, and soluble in water.
These three monosaccharides—glucose, fructose, and galactose—are crucial for nutrition. Six carbon atoms, twelve hydrogen atoms, and six oxygen atoms make up each single sugar molecule.
To learn more about monosaccharides from the given link:
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A 10.0cm3 volume of alcohol has a mass of 7.05g.
is the density
Answer: 
<u>Explanation:</u>
The ratio between the mass of a substance and its unit volume is referred as density.
is the Answer
<u>Note:</u>
1000 g = 1 kg
100 cm = 1 m
When we used to transform the given values into S.I units, then

Alcohol’s volume can be written as, 
Alcohol’s mass can denote as, 
Then, 
Answer:
chlorine, aluminum, sulfur....i think im not sure
Explanation:
Answer:
Sound waves are faster than light waves when traveling through the air.
(This statement is NOT true)
or
Sound waves and electromagnetic waves are both needed to talk on a cell phone
Explanation:
Sound waves need a medium to travel through, but light does not.
Also, the statement "Sound waves and electromagnetic waves are both needed to talk on a cell phone" might also be NOT true, since, as far as I know, cellphone calls need radio and sound waves, not electromagnetic waves.
Answer:
See explanation and image attached
Explanation:
The reaction of (R)-2-chloro-3-methylbutane with potassium tert-butoxide yields a monosubstituted alkene .
Since the base is bulky, the Hoffman product predominates because attack occurs at the less hindered carbon atom to yield the major product as shown.
The alkene reacts with HBr at the secondary carbon atom to yield a carbocation intermediate which is flat and planar. Attack on either face of the carbocation yields a racemic mixture of the (2R) and (2S) products.
Rearrangement of the carbocation to yield a tertiary carbocation gives the 2-bromo-2-methyl butane product as shown in the image attached.