The elements in Groups 1A(1) and 7A(17) are all quite reactive.
<h3>Major difference between Groups 1A(1) and 7A(17) : </h3>
Group 7's halogens, which are non-metal elements, become less reactive as you move down the group. In contrast to the alkali metals in Group 1 of the periodic table, this trend is the opposite. The most reactive element in Group 7 is fluorine.
Alkali metals are soft and reactive metals. They react vigorously with water and become more reactive. And other hand halogens are reactive non metals.
- Elements of group 1A are known as alkali metals. Elements of this group are lithium, sodium, potassium, rubidium, cesium.
- Reactivity increase down group 1 but decrease up group 7 this is because group 7 elements react by gaining an electron. As one move down the group, the amount of electron shielding increases, meaning that the electron is less attracted to the nucleus.
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Answer:
27.60 g urea
Explanation:
The <em>freezing-point depression</em> is expressed by the formula:
In this case,
- ΔT = 5.6 - (-0.9) = 6.5 °C
m is the molality of the urea solution in X (mol urea/kg of X)
First we<u> calculate the molality</u>:
- 6.5 °C = 7.78 °C kg·mol⁻¹ * m
Now we<u> calculate the moles of ure</u>a that were dissolved:
550 g X ⇒ 550 / 1000 = 0.550 kg X
- 0.84 m = mol Urea / 0.550 kg X
Finally we <u>calculate the mass of urea</u>, using its molecular weight:
- 0.46 mol * 60.06 g/mol = 27.60 g urea
Sucrose, a sweet, white crystalline substance, C12 H22 O11, OBTAINED CHIEFLY FROM THE JUICE OF THE SUGAR CANE AND SUGAR BEET, BUT ALSO PRESENT IN SORGHUM, THE sugar maple, some palms, and various other plants, and having extensive nutritional, pharmaceutical, and industrial uses; any of the class of carbohydrates to which this substance belongs, as glucose, levulose, and lactose.
Electrolysis takes place when an electric current passes through water.
Answer:
(c) The retention time would be higher (d) The retention time would be lower.
Explanation:
For the polar solutes which were separated using the hydrophilic interaction chromatography (HILIC) with a strongly polar bonded phase, the retention time would be higher if eluent were changed from 80 vol% to 90 vol% acetonitrile in water.
However, for the polar solutes which were separated using the normal-phase chromatography on bare silica with methyl t=butyl ether and 2-propanol solvent, the retention time would be lower if the eluent were changed from 40 vol% to 60 vol% 2-propanol.
