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harkovskaia [24]
2 years ago
11

Compare the electronegativity of H and O in the polar covalent bonds of a water

Chemistry
1 answer:
ExtremeBDS [4]2 years ago
7 0

Answer:

The O atom will tend to attract the electrons.

Explanation:

The electronegativity of O (3.5) is much higher than H (2.1), which means it is more likely to attract electrons. The higher the electronegativity, the more attractive.

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I’m not sure quite sure about this one please help
ehidna [41]
This one is correct
3 0
3 years ago
Which elements have the most similar chemical properties?
bixtya [17]

Answer:

a. Be and Mg

Explanation:

Be (beryllium) and Mg (magnesium) are both found in the alkaline earth metals family (group 2) on the periodic table. Elements in the same family or group have similar properties,

Ca and Br are in groups 2 and 17

Cl and Ar are in groups 17 and 18

Na and P are in groups 1 and 15

4 0
3 years ago
Read 2 more answers
Please answer he questions
Nastasia [14]

"Work done by a constant force on an object is the product of the force and the distance moved by the object in the direction of the force" -textbook

There is work done ONLY if the direction of the force and the direction the item is moving are the same. In figure A, the direction of the force (the lifting) is upwards (defying gravity), and the book is moving upwards, so work is done. In figure B, the force is still moving upwards (the person is carrying the books) but the book is moving to the right, so there is NO work done.

6 0
2 years ago
Show the mechanism for the following reaction conducted at –5 °C in CCl4: cyclohexene bromine yields a dibromocyclohexane Draw w
Darya [45]

Answer:

See attachment.

Explanation:

In the first step, a cyclic structure with a positive bromine is formed. The bromine shares the positive charge with the two carbons that it is bonded to, so the carbons are partially positive.

The second bromine atom then attacks the carbon center, coming in from below the first bromine atom ("backside attack") where the antibonding orbital of the second bromine atom is.

The stereochemistry of the mechanism causes the final product to be an anti-dibromocyclohexane.

7 0
3 years ago
Balance the following equation:
Sonbull [250]
You only need a 2 at the end In front of the NaCl
5 0
2 years ago
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