Answer:
you need only one independent variable because if not, you wont know what factors have changed your experiment.
Explanation:
Citric acid has the molecular formula C6H8O7 so you can add the molar masses of the elements from the periodic table. C has a molar mass of 12.01 g/mol, H has 1.01 g/mol and O has 15.999 g/mol. Now you calculate the total molar mass= (6*12.01 + 8*1.01 + 7*15.999). This yields a molar weight of 192.124 g/mol (anhydrous)
The mass of pentane the student should weigh out is
The density of pentane is 0.626 gcm-3
To calculate the mass of pentane following expression is used,
(Density is defined as the mass divide by volume)
Density = mass / volume
mass of pentane = Density of pentane * Volume of pentane
mass of pentane = 0.626 gcm-3 * 45.0 mL
= 28.17 g
Here the unit of mass of pentane is g,
However the unit of density is gcm-3 and unit of volume is mL i.e. cm3
Hence, Mass = gcm-3 * cm3
Mass = g
The mass of pentane the student should weigh out is 28.17g
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Answer: 1.
moles
2. 90 mg
Explanation:

According to stoichiometry:
1 mole of ozone is removed by 2 moles of sodium iodide.
Thus
moles of ozone is removed by =
moles of sodium iodide.
Thus
moles of sodium iodide are needed to remove
moles of 
2. 
According to stoichiometry:
1 mole of ozone is removed by 2 moles of sodium iodide.
Thus 0.0003 moles of ozone is removed by =
moles of sodium iodide.
Mass of sodium iodide=
(1g=1000mg)
Thus 90 mg of sodium iodide are needed to remove 13.31 mg of
.
Answer:
1) acetylide
2) enol
3) aldehydes
4) tautomers
5) alkynes
6) Hydroboration
7) Keto
8) methyl ketones
Explanation:
Acetylide anions (R-C≡C^-) is a strong nucleophile. Being a strong nucleophile, we can use it to open up an epoxide ring by SN2 mechanism. The attack of the acetylide ion occurs from the backside of the epoxide ring. It must attack at the less substituted side of the epoxide.
Oxomercuration of alkynes and hydroboration of alkynes are similar reactions in that they both yield carbonyl compounds that often exhibit keto-enol tautomerism.
The equilibrium position may lie towards the Keto form of the compound. Usually, if terminal alkynes are used, the product of the reaction is a methyl ketone.