Question

Draw the Lewis structure for 1,1 -dimethylhydrazine \(\left[\left(\mathrm{CH}_{3}\right)_{2} \mathrm{NNH}_{2},\) a compound used as a rocket fuel. \right. What is the hybridization for the two nitrogen atoms in this molecule? What orbitals overlap to form the bond between the nitrogen atoms?

Short answer

Nitrogens are sp³ hybridized, and the N-N bond forms from sp³-sp³ overlap.

Step-by-step solution

Count Total Valence Electrons

First, determine the total number of valence electrons in the molecule. Carbon (C) has 4 valence electrons, hydrogen (H) has 1, and nitrogen (N) has 5. For 1,1-dimethylhydrazine (\((CH_3)_2NNH_2\)), we have:- 2 carbons: 2 × 4 = 8- 8 hydrogens: 8 × 1 = 8- 2 nitrogens: 2 × 5 = 10Adding these together gives a total of 26 valence electrons.

Arrange Atoms and Create Bonds

Identify the central atoms. Typically the least electronegative atoms are central, but since this is an organic molecule, start with the carbon chain and then the nitrogen chain. Draw the structure in this order: C-C-N-N-H-H. Create single bonds between: - Each C and 3 H (using 6 electrons) - Each C and N (using 2 electrons) - Between the two N atoms (using 2 electrons) Total number of electrons used so far: 3×2 + 3×2 + 2 = 14.

Distribute Remaining Electrons as Lone Pairs

You now have 26 - 14 = 12 electrons left. Place these as lone pairs to satisfy the octet rule, starting with the most electronegative atom, nitrogen: - Place 3 lone pairs on the terminal N and 1 lone pair on the other N. Now, the terminal nitrogen will have full octet.

Determine Hybridization of Nitrogens

Check the geometry to find the hybridization of nitrogen atoms.- Each nitrogen has a single bond and a lone pair, creating an \(sp^3\) hybridization (tetrahedral geometry, but with lone pair reducing visual geometry to pyramidal).

Identify Orbitals for N-N Bond

In the N-N bond of the molecule, the overlapping orbitals are \(sp^3\) on both nitrogen centers, as both nitrogen atoms are \(sp^3\) hybridized.

Key concepts

Hybridization

Hybridization is a concept that helps explain the structure and bonding of molecules. In 1,1-dimethylhydrazine, the nitrogen atoms are hybridized to accommodate the surrounding atoms and lone pairs. Let's explore why each nitrogen atom in this molecule exhibits \( sp^3 \) hybridization. This type of hybridization occurs when one \(s\) orbital and three \(p\) orbitals mix to form four equivalent \(sp^3\) hybrid orbitals.

• Each nitrogen atom in the molecule forms three sigma bonds – two with carbon and one with the other nitrogen atom.
• 'Plus' each nitrogen atom has a lone pair of electrons.

This configuration prompts each nitrogen atom to adopt an \(sp^3\) hybridization, resulting in a tetrahedral arrangement around each nitrogen. However, due to the presence of the lone pair of electrons, the visible geometry appears as trigonal pyramidal, with the lone pair creating asymmetry. This hybridization is key to understanding the molecular shape and bonding properties of the nitrogen atoms in the molecule.

Valence Electrons

Valence electrons play a vital role in determining how atoms bond in a molecule. They are the outermost electrons and are crucial for forming chemical bonds. For 1,1-dimethylhydrazine, calculating the total number of valence electrons is the first step in constructing its Lewis structure.

• Each carbon atom contributes 4 valence electrons.
• Each hydrogen atom contributes 1 valence electron.
• Each nitrogen atom contributes 5 valence electrons.

Adding these together, there are a total of 26 valence electrons to be distributed within the molecule [(2 carbons) x 4 + (8 hydrogens) x 1 + (2 nitrogens) x 5 = 26]. These electrons are initially arranged to form the bones of the structure, which involves single bonds between atoms. Once these skeleton bonds are in place, the remaining electrons are assigned as lone pairs, primarily on nitrogen, to satisfy the octet rule. Understanding valence electrons is crucial as they influence the molecular geometry and reactivity.

Organic Molecule

1,1-Dimethylhydrazine is an organic molecule featuring carbon atoms bonded with nitrogen and hydrogen atoms. Organic molecules typically contain carbon atoms in chains or rings connected by various covalent bonds. Being an organic compound, 1,1-dimethylhydrazine is made up of the basic elements found in organic chemistry:

• Carbon (C): Essential in creating the 'backbone' of the molecule.
• Nitrogen (N): Provides additional bonding sites and influences hybridization.
• Hydrogen (H): Completes the molecule's structure and stabilizes it.

The presence of nitrogen atoms introduces special attributes, like forming stable bonds and hybridizing to adjust their bonding capabilities. Moreover, understanding the fundamental characteristics of organic molecules aids in explaining important theoretical concepts such as isomerism and molecular geometry, which are relevant when discussing molecules like 1,1-dimethylhydrazine.

Nitrogen Bonding

Nitrogen bonding is a fundamental aspect of many chemical compounds. In the context of 1,1-dimethylhydrazine, we explore the nitrogen-nitrogen bond as well as the bond between nitrogen and other atoms in the molecule.Nitrogen atoms typically form three covalent bonds due to having five valence electrons:

• Two nitrogen atoms form a single bond with each other in 1,1-dimethylhydrazine, leading to a shared pair of electrons.
• Each nitrogen engages in single bonds with carbon and hydrogen atoms.

The nitrogen-nitrogen bond involves \(sp^3\) hybridized orbitals on each nitrogen atom, as identified by the overlapping orbitals contributing to the sigma bond. The presence of nitrogen influences molecular geometry and properties, often leading to angular geometries and influencing reactivity. Understanding nitrogen bonding helps in predicting molecule behavior, enabling chemists to create compounds for specific applications, like rocket fuels.