Warning: foreach() argument must be of type array|object, bool given in /var/www/html/web/app/themes/studypress-core-theme/template-parts/header/mobile-offcanvas.php on line 20

In which of the following diatomic molecules would the bond strength be expected to be weaken as an electron is removed?

a. H2

b. B2

c. C22-

d. OF

Short Answer

Expert verified

The weakest bond strength is for option b

The bond strength depends upon the bond order.

The greater the bond order more is the bond strength

The bond order is12(nb-na)

Where

role="math" localid="1663770311020" nb=bondingelectronsna=noofantibondingelectron

Step by step solution

Achieve better grades quicker with Premium

  • Unlimited AI interaction
  • Study offline
  • Say goodbye to ads
  • Export flashcards

Over 22 million students worldwide already upgrade their learning with Vaia!

01

Step 1

On removing an electron, H+2(1electron) is formed

So the bond filling is σ11s

And the bond order is B.O=12

On removing an electron is formed B+2(9e-)

So bond filling is σ21s(σ*1s)2(σ2s)2(σ*2s)2π12px

And the bond order is

localid="1663770859533" B.O=12(5-4)B.O=0.5

For c) on removing an electron C2-(13e-) is formed

Bond filling order is σ21s(σ*1s)2(σ2s)2(σ*2s)2π22pxπ22pyσ12pz

Bond order is

localid="1663772662156" B.O=12(9-4)B.O=2.5

For d) on removing an electron OF+(16e-)

The bond filling is as follows σ21s(σ*1s)2(σ2s)2(σ*2s)2σ22pzπ22pxπ22pyπ*2pzπ2py*

Bond order is

B.O=12(10-6)B.O=2

02

Step 2

The bond order of B2 on removing an electron is the lowest so it will have the weakest bond strength.

Final answer:

The weakest bond strength is for option b

One App. One Place for Learning.

All the tools & learning materials you need for study success - in one app.

Get started for free

Most popular questions from this chapter

Show how a dxz atomic orbital and a pz atomic orbital combine to form a bonding molecular orbital. Assume the x - axis is the internuclear axis. Is a σor a πmolecular orbital formed? Explain.

Consider the following computer-generated model of caffeine:

Complete a Lewis structure for caffeine in which all atoms have a formal charge of zero (as is typical with most organic compounds). How many C and N atoms are sp2 hybridized? How many C and N atoms are sp3 hybridized? sp hybridized? How many sigma and pi bonds are there?

Why are d orbitals sometimes used to form hybrid orbitals? Which period of elements does not use d orbitals for hybridization? If necessary, which d orbitals (3d, 4d, 5d, or 6d) would sulphur use to form hybrid orbitals requiring d atomic orbitals? Answer the same question for arsenic and for iodine.

Using the molecular orbital model to describe the bonding inF2+,F2,F2- predict the bond order and the relative bond length for these species. How many unpaired electrons are present in each species?

For each of the following chemical formulas, an NMR spectrum is described, including relative overall areas (intensities) for the various signals given in parentheses. Draw the structure of a compound having the specific formula that would give the described NMR spectrum. Hint: All of these formulas represent organic compounds. Lewis structures for organic compounds typically have all atoms in the compound with a formal charge of zero. This is the case in this problem.)

a.C2H3Cl3;NMRhas one singlet signal.

b.C3H6Cl2;NMRhas a triplet (4) and a quintet (2) signal.

c.C3H6O2; NMR has a singlet (1), a quartet (2), and a triplet (3)signal.

d.C5H10O; NMR has a heptet (1), a singlet (3), and a doublet (6) signal.

e.C3H6O;NMRhas a triplet (3), a quintet (2), and a triplet (1) signal.

See all solutions

Recommended explanations on Chemistry Textbooks

View all explanations

What do you think about this solution?

We value your feedback to improve our textbook solutions.

Study anywhere. Anytime. Across all devices.

Sign-up for free